Quality Control Analyst Jobs in Maryland

Microbiology Laboratory Technologist Serve as a laboratory technician performing laboratory procedure and experiments as required. Compensation & Benefits: Estimated Starting Salary Range for Lab Technician: $60,000 to $70,000 Pay commensurate with experience. Full time benefits include Medical, Dental, Vision, 401K and other possible benefits as provided. Benefits are subject to change with or without notice. Lab Technician Responsibilities Include: Serve as a laboratory technician working under the supervision of a principal investigator (Research/Clinical Scientist) or contractor laboratory manager/supervisor in performing laboratory procedure and experiments as required for the phenotypic and genotypic characterization of MDRO Perform experimental work including serological assays, chemical assays, genetic and molecular biology procedures, growth of solid and liquid cultures Perform routine laboratory duties required for the smooth and safe operation of laboratory such as maintaining a supply of clean glassware, properly disposing of hazardous biological and chemical waste, preparing reagents, and maintaining an inventory of laboratory chemicals Collect and process blood specimens from submitting laboratories Send the shipping supplies to submitting facilities and laboratories Verify analytic accuracy, precision, sensitivity and references ranges for test methods Work with Physician to analyze results and conduct more difficult, non-routine tests Maintain a laboratory notebook in which accurate and complete records of laboratory work is maintained in accordance with accepted standards Follow laboratory SOPs and specific written experimental protocols as well as oral instructions in performing assigned experimental work Submit reports and data summaries when applicable Comply with occupational health and safety standards and other applicable regulations and guidelines which may include medical surveillance Participate in the development of research protocols and grant proposals and in the conduct of research related to MRSN activities Attend relevant seminars, scientific conferences and meetings to the MRSN Operate systems/methodologies in order to produce timely and accurate data for patients, Quality Control (QC), and proficiency testing Ensures quality specimens for laboratory testing Report clinical data accurately and efficiently to ensure givers receive timely patient information Works to improve and expand the skill set of others involved with this effort by communicating and maintaining team knowledge Performs other job-related duties as assigned Lab Technician Experience, Education, Skills, Abilities requested: AS or BS in Biology, Chemistry or Microbiology 1-3 years of experience in clinical microbiology or molecular biology outside of an academic setting Familiarity with the processing of microbial identification and antibiotic susceptibility testing data generated on the three most widely used automated systems: Phoenix, Microscan, and Vitek2 Strong teamwork and collaboration abilities Ability to work in a fast-paced environment using critical thinking skills and decisive judgement with minimal supervision Ability to perform work that requires frequent standing, walking, lifting, grasping and repetitive motion. Lifting up to 50 pounds Occasional stooping, squatting, pushing, pulling climbing, and overhead lifting Must possess an active Medical Laboratory Technician (MLT) or Medical Technician (MT) certification Must pass pre-employment qualifications of Cherokee Federal Company Information: Cherokee Nation Operation Solutions (CNOS) provides support, services, and solutions to federal and commercial customers. The company takes a personalized approach to solving our clients' toughest challenges, helping you make the most of your skills. CNOS is part of Cherokee Federal - a team of tribally owned federal contracting companies. For more information, visit cherokee-federal.com. Laboratory Technologist Clinical Lab Technician Research Lab Technician Molecular Biology Technician Microbiology Lab Assistant Laboratory technician Microbiology Molecular biology Clinical lab Antibiotic susceptibility testing Legal Disclaimer: Cherokee Federal is an equal opportunity employer. Please visit cherokee-federal.com/careers for information regarding our Affirmative Action and Equal Opportunity Employer Statement, Accommodation request, and Presidential EO 14042 Notice.

We are seeking a Chemist to support the development of biopharmaceutical products, including monoclonal antibodies and antibody drug conjugates. The role involves performing analytical testing and method development using Chromatography and Electrophoresis techniques. Key Responsibilities: Conduct analytical testing and method development. Make detailed experimental observations and analyze data. Interpret results and prepare summaries for presentations and reports. Qualifications: Experience in a chemistry or biochemistry laboratory. Familiarity with protein chemistry and at least one analytical technique (chromatography or electrophoresis). Mass spectrometry experience is a plus. Experience with data analysis software (e.g., Empower, Openlab) is desirable. Strong teamwork, communication, multi-tasking, and organizational skills. Top Requirements: Experience with HPLC. Knowledge of large molecules. Understanding of antibody drug conjugates (ADCs).

Zentech is one of the leading and most highly certified U.S. based Electronics Manufacturing Services (EMS) providers in North America. We support original equipment manufacturers (OEMs) of medical devices, aerospace and defense products, and industrial equipment with engineering & manufacturing solutions. These solutions include product design, printed circuit board layout, test development, and manufacturing support through the whole product lifecycle. The products and designs Zentech support are an integral part of everyday life and in mission critical environments. Many can be seen every day at sporting events, on delivery trucks, in medical offices, at construction sites, on American farms, and on commercial aircraft. Other products and designs are unseen but vital, such the work we do for our domestic and foreign military customers who rely on our technical skills to help ensure our country remains safe, our warfighters remain out of harm's way, and our nation's networks remain free from intrusion. Zentech has developed strengths in the required manufacturing processes for high reliability, high complexity, low-to-medium volume printed circuit boards and box builds, all with best-in-class ability to scale to higher volume products. Zentech products are proudly Made in America. Job Description: The Quality Control Inspector performs product inspections utilizing magnified visual aids and mechanical measuring devices to ensure product conformance to internal and customer technical data package requirements. This process includes analyzing technical data packages (e.g. assembly instructions, engineering drawings, schematics, bills of material, specifications, etc.) in order to: Identify and resolve issues affecting product configuration Identify and assign rework actions necessary to rework production product Accept production product work-in-process and approve for next assigned operation Skills: Candidates must be able to work in a self directed manner in a fast-paced working environment Foster and maintain professional and productive relationships with other staff and management Possess excellent verbal and written communication skills Demonstrate proficiency in computer based applications Have experience with electronic assembly including; SMT, T/H & Mechanical Ability to effectively operate visual magnification devices (scope) Ability to effectively operate and interpret basic electronic measuring devices Ability to effectively operate and interpret basic mechanical measuring devices Qualifications: High school diploma or equivalent required, some college preferred Basic math skills required Acceptable visual acuity and eye-hand coordination Must have, or be able to acquire, operator certification for IPC-A-610 Must have, or be able to acquire, operator certification for J-STD-001 Ability to review and interpret technical data packages for electronic assemblies Physical Demands: While performing these duties, the employee is required to sit or stand for extended periods of time, reach with hand and arm, and talk or hear. Employee may be required to lift up to 50 pounds. Zentech Manufacturing is an Equal Opportunity Employer. Zentech will recruit, hire, train, and promote persons in all job titles without regard to real or perceived classification of race, ethnicity, ancestry, color, marital status, religion, national origin, veteran status, sex, sexual orientation, genetic information, gender identity or expression, age, or physical or mental disability. PIbd9a3ccbf5c8-26***********2

The Quality Control Technician II is responsible for accurately reviewing work by other departments to ensure all steps were taken, paperwork was properly completed, and calls were properly addressed and handled. A Quality Control Technician II is responsible for checking 3 or more departments for quality. ESSENTIAL JOB DUTIES AND RESPONSIBILITIES* · Review work product of team members at set percentages, records accuracy and provides feedback. · Summarize data in spreadsheets to provide to department Supervisor and/or Manager. · Review steps taken by employee by either reading or listening to process steps taken. · Read steps in AS400, client systems and/or outgoing mail to ensure proper client procedures taken. · Listen to calls and review account in AS400 to ensure accurate steps taken per client procedures and state law. · Obtain outgoing work from teams without disruption. · Lift tubs of work up to 25 lbs. · Make suggestion for changes to the QC process. · Identify errors trends. MINIMUM JOB SKILLS, ABILITIES AND QUALIFICATIONS · Pass applicable pre-screen testing. · Mastery of the English language, both written and verbal. · Strong attention to detail, is dependable and follows through. · Ability to analyze data and present recommendations based on outcomes of analysis. · Ability to use Microsoft Excel and various function available in Excel. · High level of maturity to handle sensitive and confidential situations. · Discuss in detail performance of quality with Supervisors / Managers. · Strong work ethic andexcellent time management skills. · Strong interpersonal skills and ability to work well with people throughout the organization. · Willingness to maintain a professional appearance and provide a positive company image. · Ability to perform under minimal supervision. · Ability to understand key functions of departments responsible for QC. · Mathematical skills to determine volume to QC from percentage expected for QC. · Ability to meet expected production guidelines Desired Skills and Experience MINIMUM JOB SKILLS, ABILITIES AND QUALIFICATIONS · Pass applicable pre-screen testing. · Mastery of the English language, both written and verbal. · Strong attention to detail, is dependable and follows through. · Ability to analyze data and present recommendations based on outcomes of analysis. · Ability to use Microsoft Excel and various function available in Excel. · High level of maturity to handle sensitive and confidential situations. · Discuss in detail performance of quality with Supervisors / Managers. · Strong work ethic andexcellent time management skills. · Strong interpersonal skills and ability to work well with people throughout the organization. · Willingness to maintain a professional appearance and provide a positive company image. · Ability to perform under minimal supervision. · Ability to understand key functions of departments responsible for QC. · Mathematical skills to determine volume to QC from percentage expected for QC. · Ability to meet expected production guidelines. All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

Job Title: Research & Development Chemist Department: R&D Reports To: Vice President of R&D ______________________________________________________________________________ This is a laboratory-based position that will aid in improving our various water analysis products as well as help design and implement new products. Job Responsibilities: Works safely Develops new and improved reagents and products. Develops formulations for tableted or powdered reagents Develops formulations for liquid and dried reagents Develops formulations for test strip reagents Ability to perform reagent calibrations on colorimeter/photometers Ability to use spread sheets and other data analysis applications Provides technical assistance to Customer Service and Marketing personnel. Resolves technical problems. Provides technical support to QC, QA, to resolve problems. Performs related laboratory duties as assigned. Conducts performance evaluations of our products versus competitor's products of similar specifications. Prepares calibration standards for checking performance of instruments. Provides technical input for quotations and product costs. Provides technical input for the preparation of SDS, instructions and labels. Maintains laboratory notebook and/or electronic notes and records. Prepares pre-production batches of reagents to establish specifications. Writes SOPs, TIs, operation instructions and manuals as needed. Participates in staff meetings as needed. Miscellaneous: Participates in lean activities, including but not limited to Lean training and lean events such as kaizen or a 5-day event. 5-S program in the various departments assigned. DMAICs. Continuously looks for ways to improve both departments' and own individual efficiencies and time management, as well ways to improve any aspect of the Company's operations and develops and implements DMAICs accordingly. Notifies Manager of any production, equipment, safety or personnel problems, etc. and cooperates in resolving such issues as well. For example, requests assistance when systems prevent the efficient performance of duties or when a system fails. Provides Manager with feedback to determine where additional training would benefit and obtains additional training as necessary. Complies with all Company policies (i.e. personnel, safety, etc.). Performs other duties as assigned. (Such duties may or may not be essential functions of the job. Qualifications/Requirements: Requires a minimum of B.S. or B.A. degree in chemistry from an accredited institution, with 2 or more years of lab experience in chemistry or a related field (i.e. biochemistry), and/or an advanced degree in chemistry or pharmaceutical chemistry. Must have good laboratory skills to safely handle chemicals and instruments used in R&D laboratory, be familiar with computer-assisted instrumentation, possess good color perception and adequate manual dexterity, maintain accurate records, work according to established laboratory procedures, work independently without requiring day-to-day supervision and have proficient computer skills using Microsoft Office at a minimum, additional computer skills with data analysis applications an advantage. Environmental Factors/Physical/Mental Capabilities: Works indoors in temperature controlled environment.Handles various chemicals. Requires good problem solving, judgment, communication skills, math skills and color perception. Requires walking, standing, sitting, good manual dexterity and some transporting up to 30 lbs. LaMotte Company, a 100+ year-old global industry leader in developing and manufacturing premier water analysis solutions, operating in Newark, DE, Chestertown, MD and Warwick, UK. Our products are used around the world to accurately, quickly, and conveniently test water in a multitude of applications. LaMotte offers paid time off including vacation, sick leave, and paid holidays. Full-time employees, who regularly work at least 30 hours per week, are eligible for employer-provided insurance including health, dental, vision, disability, life insurance, and supplemental insurance. Full-time employees are eligible to contribute to our 401(k) plan with an employer match available. LaMotte is committed to a policy of Equal Employment Opportunity and will not discriminate against an applicant or employee on the basis of race, color, religion, creed, national origin or ancestry, sex, age, disability, military status, genetic information, sexual orientation, or any other legally recognized protected basis under federal, state, or local laws.

Catalent Pharma Solutions Location: Harmans, Maryland Type: Non-Remote Posted on: November 11, 2024 {"job PostingInfo":{"id":"485405ca20a51001ec5482151e5e0000","title":"Senior QC Scientist, QC Moda Administrator","job Description":" The Senior QC Scientist, QC Moda Administrator responsibilities include technical support, configuration, administration, training and maintenance of the MODA application and those peers that use the software. The individual may be asked to participate/ assist in supporting internal projects and application updates as necessary. Furthermore, this position may participate in internal and external audits. Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee. The role: • Manages and maintains MODA while ensuring regulatory compliance. • Builds and manages data as necessary for the QC EM department. • Supports internal and external projects within the application. • Develops and provides training to end users as necessary. • Experience with System Design and development to ensure delivery of quality results. • Perform or aid in Periodic User Access Reviews and Periodic Audit Trail Reviews of the MODA application. • Effective communication with Quality Instrumentation Manager regarding status of daily work. • Other duties as required in support of Catalent Pharma Solutions high performance, such as but not limited to, assisting site management in driving and enforcing cGMPs; mentoring other individuals within the application of MODA. • Drive improvements and efficiencies in the MODA process. The candidate: • Bachelor's degree in science or related field required (Information Technology (IT), Chemistry, Microbiology or Biology preferred) or three to six years of MODA Administration and/or builder experience • Ability to effectively present information and respond to questions from peers, management, regulatory and customers. • Maintain and update associated standard operating procedures (SOPs) as necessary. • Strong knowledge of Computerized System Validation (CSV). The anticipated salary range for this position in Maryland is $93,280-$128,260 plus an annual bonus. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states. Why you should join Catalent: • Competitive medical benefits and 401K • 152 hours PTO + 8 Paid Holidays • Dynamic, fast-paced work environment • Opportunity to work on Continuous Improvement Processes Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE . 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Employee Type: Full time Job Type: Production Operations Job Posting Title: QC Technician-2 About Us: TreeHouse Foods (NYSE: THS) is a leading manufacturer of private label packaged foods and beverages, operating a network of production facilities across the United States and Canada. At TreeHouse Foods, our commitment to excellence extends beyond our products and revolves around our people. We are investing in talent and creating a performance-based culture where employees can do their best work, directly impacting our mission to make high quality, affordable food for our customers, communities and families. We hope you will consider joining the team and being part of our future. What You Gain: Competitive compensation and benefits program Enrollment in our wellness and employee assistance programs Paid holidays, vacation, and other competitive paid time off opportunities An inclusive working environment where you can build meaningful work relationships with a diverse group of people Leaders who are invested in supporting your career growth Opportunities to be recognized for outstanding contributions to your team through our employee recognition programs Job Description: Perform routine testing of raw materials, in-process products, and finished goods to ensure compliance with quality and safety standards. Conduct environmental monitoring, including sampling and testing for aseptic conditions. Perform checks on packaging, labeling, and coding for accuracy and compliance. Operate, calibrate, and maintain laboratory equipment according to standard operating procedures (SOPs). Document test results, inspections, and non-conformance findings accurately and legibly. Assist in root cause analysis and corrective actions for quality deviations or non-conformances. Verify cleanliness and sanitation of equipment and production areas before operations begin. Monitor critical control points (CCPs) and ensure compliance with Hazard Analysis Critical Control Point (HACCP) and other regulatory programs. Conduct Good Manufacturing Practices (GMP) audits to ensure facility standards are upheld. Collaborate with production teams to identify and resolve quality issues in real-time. Maintain a safe and clean work environment by adhering to company policies and procedures. Participate in continuous improvement initiatives to enhance quality systems and processes. Support internal and external audits as required. Perform other duties as assigned by the Lead/Quality Supervisor. Education and Experience: High School Diploma or GED required; an Associate's degree or higher in Food Science, Microbiology, or a related field is preferred. Prior experience in quality assurance or quality control within the food manufacturing industry is highly desirable. Skills and Abilities: Strong attention to detail and organizational skills. Basic understanding of aseptic processes, HACCP, GMP, and FDA/USDA regulations. Proficient in data entry and documentation, with basic computer skills (e.g., Microsoft Office, ERP systems). Ability to work independently and as part of a team. Excellent communication skills to effectively relay quality concerns to production staff and management. Why Join Us? Be a vital part of maintaining the highest standards of food safety and quality in a fast-paced, innovative aseptic food manufacturing facility. If you're detail-oriented and passionate about quality, we'd love to have you on our team! Your TreeHouse Foods Career is Just a Click Away! Click on the “Apply” button or go directly to ****************************** to let us know you're ready to join our team! At TreeHouse Foods, we embrace diversity and inclusion for innovation and growth. We are committed to building inclusive teams and an equitable workplace for our employees to bring their true selves to work to help us “Engage and Delight - One Customer at a Time”. TreeHouse Foods is an Equal Opportunity Employer that prohibits discrimination or harassment of any type. All qualified applicants are considered for employment without regard to race, color, national origin, age, sex, sexual orientation, gender, gender identity or expression, disability status, protected veteran status, or any other characteristic protected by law. Applicants who require an accommodation to participate in the job application or hiring process should contact disability-accommodations@treehousefoods.com TreeHouse Use Only: #IND1

The Associate Quality Control Analyst will be responsible for completion of specification testing and related laboratory tasks to schedule to ensure raw materials and finished products meet company and/or customer quality expectations. Core Responsibilities: Operate and maintain a safe, clean and accident-free laboratory environment. Prioritize testing based on business needs and departmental goals. Perform specialized testing in support of internal and external customers and departmental projects. Ensure non-routine testing is performed in an appropriate manner. Calibrate and maintain laboratory instruments, ensure that necessary laboratory supplies and equipment are available. Maintain complete and accurate records of laboratory data. Review laboratory data for accuracy; communicate concerns and nonconformances to laboratory supervisor. Develop a working knowledge of products and customer requirements. Maintain sample retain library. Participate in Improvement of Quality Assurance and Food Safety systems through continuous improvement activities. Manage release timeframe of inbound raw materials and finished goods by monitoring Review outstanding testing of products in QI status. Participates in facility GMP audits Implement corrective actions agreed upon by laboratory management as a result of laboratory investigations or proficiency testing and monitor their effectiveness. Stay current with scientific developments in areas of expertise and responsibility. Work with operations and quality assurance to understand current demands on laboratory services. Work with Operations to identify, investigate, and resolve process discrepancies. Perform other work as assigned. Qualified candidates will have: Bachelor's Degree in Chemistry, Food Science or related field. Desire to work in a fast-paced, team environment Analytical, organized, and detailed oriented Strong communication and math skills Availability to work weekend shifts, as needed, on a rotating basis We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Ingredion provides accommodations to job applicants with disabilities throughout the hiring process. If a job applicant requires an accommodation during the application process or through the selection process, we will work with the applicant to meet the job applicant's accommodation needs. We are an equal opportunity employer and value diversity at our company. Ingredion seeks to provide a work environment that is free from harassment and discrimination. We will not tolerate any form of discrimination based on race, color, religion, age, gender, gender identity, gender expression, national origin, ancestry, handicap or disability-mental or physical-marital status, sexual orientation, veteran status, disability resulting from military service, or any other classification protected by law (“protected classifications”). We are committed to establishing and maintaining a work environment where everyone is treated with dignity and respect. Ingredion provides accommodations to job applicants with disabilities throughout the hiring process. If a job applicant requires an accommodation during the application process or through the selection process, we will work with the applicant to meet the job applicant's accommodation needs. Relocation Available: No Pay Range: $48,300.00-$64,433.33 Annual This pay range is not a guarantee of compensation or salary. Final base salary will be determined based on several factors which may include but are not limited to responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data and applicable bargaining agreement (if any). Incentive Compensation: As a part of the total compensation package, this role may be eligible for the Ingredion Annual Incentive Plan or a role-specific commission/bonus. Benefits: Full-time roles are eligible for our comprehensive benefits package which includes medical, dental and vision coverage as well as a 401(k) plan with an competitive company match.

Share If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. **QA Associate- Supplier Qualification** Full Time Clerical 8 days ago Requisition ID: 1465 Salary Range: $25.00 To $35.00 Hourly **Job Overview:** The QA Associate ensures compliance with cGMP and internal policies, procedures, and specifications. This position is responsible for performing a role in any one or more of the following functions: Quality Operations, Process Quality, Batch Release, Quality Systems, and Compliance in accordance with cGMP and related company SOPs, state, federal and local laws as applicable. **Responsibilities:** * To complete quality assurance tasks as directed by the supervisor associated with the review of operations performed within the site. These may include product release, process quality, quality systems & operations, and compliance. * To support or contribute to the preparation, review, and approval of QA-related documentation in accordance with approved SOPs. * To perform or assist in general organizational tasks including oversight and escalation of open tasks and timelines, tracking of tasks, generation of technical reports, and reporting of quality metrics. * To ensure that appropriate quality standards are applied in accordance with regulatory, pharmacopeias, and company requirements. * To assist in quality-related activities that may include the preparation and review of GMP documentation. * To escalate compliance issues appropriately when discovered. * To complete assigned training in a timely fashion to ensure that both personal and department training status remains current. * Review data to ensure conformance to product specifications and maintain quality assurance objectives to meet regulatory requirements. * Respond to external customers. * Perform other duties as assigned. **Qualifications:** * Bachelor's degree, or equivalent combination of education, training and professional experience that provides the individual with the required knowledge, skills, and abilities. * Minimum of 3+ years of Quality Assurance experience in a GMP-regulated industry, such as pharmaceutical, biologics, medical devices, or in combination with relevant education * Demonstrate the ability to establish good working relationships with other departments, including vendors, colleagues, and subordinates. * Demonstrates the appropriate technical knowledge necessary to make sound decisions on development issues with minimal supervision. * Demonstrate the ability to analyze data and information and assess and resolve complex problems/issues as required. * Must be able to comprehend and follow all applicable SOPs. * Demonstrate knowledge and experience with electronic Quality Management Systems such as MasterControl and Trackwise. * Demonstrate understanding/ability to acquire the appropriate knowledge from resources on the current federal, local, and international regulations regarding the production, testing, and release of drug substances and products. * Good understanding of cGMPs, industry, and regulatory standards and guidelines. * Demonstrate familiarity with Microsoft programs like Word, Excel, PowerPoint, Project, Teams, Outlook, etc. * Demonstrate the ability to portray the appropriate level of integrity and professionalism. * Demonstrate the ability to communicate effectively with management, staff, regulators, and client representatives in written and verbal formats. * Demonstrate the ability to complete tasks accurately and according to established and shifting timelines. * Demonstrate the ability to make quality scheduling, resource allocation, and priorities decisions. * Energetic, execution-focused, self-motivated, and organized individual who is accustomed to working in a deadline-focused, high-pressure entrepreneurial environment. * Results-oriented and efficient. * Creative and open-minded who fosters an environment in which sharing of ideas is encouraged. * Demonstrate the ability to work closely with a diverse customer and employee base (internally and externally). * Demonstrate the ability to work well in a cross-functional team environment. * Must communicate fluently in English and have legible handwriting. **Physical Demands:** * Ability to travel between and within facilities to visit staff, operations, and projects, as needed. * Ability to sit, stand, climb stairs, and climb ladders to mezzanines (when necessary). * Ability to lift up to 40 pounds on occasion. * Ability to use PPE (safety shoes, goggles, respirators, gloves, etc. when necessary).

The **LIMS Administrator** will be responsible for account management and implementation within the LabVantage Laboratory Information Management System (LIMS) implemented at the Catalent Pharma Solutions, BWI Harmans site. This position will be responsible for providing end-user support for all analytical groups as well as compliance to global Catalent and internal policies and procedures. Additionally, the LIMS Administrator may be tasked to participate in a global/local process for general or Catalent Global applicable design modifications. Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee. **The role:** * Administer accounts, roles and system function per global/local LIMS procedures. * Solve end-user LIMIS template and end-users LIMS data entry issues. * Work with IT and Quality personnel to ensure system compliance. * First-line support for end-user LIMS template and data entry issues. * Assist in the development and implementation of a site process for the scheduling and status tracking of all site LIMS Master Data, including needs for Raw Material, Finished Goods, and Stability testing. * Work to maintain site and Catalent Global requirements of LIMS. * Maintain and update site and/or Catalent Global Standard Operating Procedures (SOPs). **The candidate:** * Bachelor's degree from four-year college or university in any of the following disciplines: Pharmacy, Biology, Chemistry, Engineering, Information Technology or related discipline * 5+ years of experience in the Pharmaceutical or Biotech industry or relevant business experience. * Experience with LIMS or Material Management System is preferred. * Knowledge of cGMPs and other regulatory requirements relative to LIMS system and validation procedures is preferred. * Knowledge of the use of LIMS in a pharmaceutical laboratory, preferably LabVantage LIMS is preferred. The anticipated salary range for this position in Maryland is $93,280-$128,260 plus an annual bonus. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states. **Why you should join Catalent:** * Competitive medical benefits and 401K * 152 hours PTO + 8 Paid Holidays * Dynamic, fast-paced work environment * Opportunity to work on Continuous Improvement Processes **Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit to explore career opportunities. Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to ***************** for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice .

We are looking for a hands-on, laser-focused Quality Control Technician with excellent attention to detail, that will be able to inspect product for quality and reliability. ResponsibilitiesRead and interpret component drawings, material specifications, process specifications and work instructions.Perform visual and dimensional inspections on incoming products and internally manufactured products.Record inspection and test data / prepare documentation records for manufactured products.Maintain inspection, production and lot traceability records.Evaluate inspections, test data, documentation and report deviations from existing standards using the nonconformance reporting system.Maintain tool and equipment calibration control process.Assist with shipping and receiving activities.Develop/Write Inspection Plans or Inspection Work Instructions RequirementsHigh School Diploma or GED, some vocational or technical training preferred.Minimum of 3-5 years of directly related experience, and/or equivalent combination of education and experience in a related field. Basic knowledge of & experience working within an ISO 9001 / AS9100 Quality Management SystemStrong mechanical background desirable, with experience working within a manufacturing and assembly environment.Proficient with the use of various measurement devices such as micrometers, calipers, height gage and coordinate measuring machine Ability to apply basic mathematical skills and Statistical Process Control methods to assist with the inspection process.Proficiency using MS Word and ExcelExperience with Government project work highly desired. $55,000 - $65,000 a year

The Analyst II, QC Microbiology position supports the Quality Control group to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the Microbiology, Environmental Monitoring, and Utility testing programs, which includes microbiological product testing, monitoring of the manufacturing production space, and supporting quality initiatives. The individual routinely conducts monitoring, testing, and SOP generation and revision. ESSENTIAL FUNCTIONS Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. Perform various microbiological testing procedures as per Manufacturing/Quality Control batch records, stability protocols, raw material requests for testing, etc. Perform environmental monitoring and utility testing of the facility. Performs environmental monitoring during fill operations. Work with Project Managers and QA to ensure timely testing and release of samples. Inform supervisor/manager upon observing OOS, OOL, or generation of deviations Participate in investigations of OOS results and other related studies. Participate in validation, troubleshooting various types of equipment including proactive resolution of instrument issues. Investigate and suggest new laboratory procedures/techniques. Validate and implement new laboratory procedures/techniques. Update existing or write new testing standards and standard operating procedures. Train Microbiologist I & II in methods and techniques Review, analyze, interpret and report data. Practice Good Documentation and Laboratory Safety Procedures per the Standard Operating Procedures. Support department compliance and productivity goals. Write and review monthly reports as necessary Track time worked per project. Participate in and attend professional seminars, conferences and conventions. The above statements are intended to describe the nature of work performed by those in this job and are not an exhaustive list of all duties. Nothing in this job description restricts managements right to assign or reassign duties and responsibilities to this job at any time which reflects management's assignment of essential functions. III. MINIMUM EDUCATION, EXPERIENCE, SKILLS To perform the job successfully, an individual should demonstrate the following competencies to perform the essential functions of this position. Technical/Professional Knowledge having achieved a satisfactory level of technical and professional skill or knowledge in position-related areas;keeping up with current developments and trends in areas of expertise. Problem Solving the individual identifies and resolves problems in a timely manner and gathers and analyzes information skillfully. Safety and Security the individual observes safety and security procedures and uses equipment and materials properly. May be required to lift items that are approximately 25lbs. Communication the individual speaks clearly and persuasively in positive or negative situations, demonstrates group presentation skills and conducts productive meetings. Quality Management the individual looks for ways to improve and promote quality and demonstrates accuracy and thoroughness. Planning/Organizing the individual prioritizes and plans work activities, uses time efficiently and develops realistic action plans. Adaptability maintains effectiveness when experiencing major changes in work tasks or the work environment;adjusting effectively to work within new work structures, processes, requirements, or cultures. Stress Tolerance maintaining stable performance under pressure or opposition (such as time pressure or job ambiguity);handling stress in a manner that is acceptable to others and to the organization. Education: BS in Microbiology/Biology or related field Experience: Minimum 2-4 years (MS with 0-2 years) in the Pharmaceutical or Biotechnology with emphasis in one of the following areas: aseptic processing, QC microbiology, environmental monitoring, water system, quality control, validation and manufacturing processes. Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws. By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.

- **Quality Control Chemist I** Contract: Fredrick, Maryland, US Salary: $35.00 Per Hour Job Status: Expired **This Job is no longer accepting applications** **Job Description:** **Job Roles & Responsibilities:** **To discuss more about this job opportunity, please reach out to Chitrank Rastogi (LinkedIn URL - ********************************************************* email your updated resume at Email - ****************************** or give me a call at **************. Thank you!** **Pay Range - $30 to $35/hr. (negotiable)** **Responsibilities (include but are not limited to):** * Perform testing of raw materials, intermediates and final products by following analytical methods: Cell based bioassays, Flow Cytometry, ELISA and qPCR assays. * Work with internal and external resources to maintain lab in an optimal state. * Assist with monitoring and trending data, complete routine record review of test data and related documents for in-process testing, drug substance and drug product release. * Supply information to support generation of CoAs for product release. * Maintains laboratory instruments for calibration and routine maintenance * Author or revise SOPs, qualification/validation protocols and reports. * Assist with lab investigations regarding out of specifications (OOS) results. * Participate in determination of root cause for deviations related to analytical procedures. * Provide updates at daily and weekly meetings. * Monitor the GMP systems currently in place to ensure compliance with documented policies. * Review proposed changes to systems, procedures, methods, and submissions to regulatory agencies, as appropriate. * Gather metric information for use in continuous improvement of areas of responsibility. * Perform other duties as required. **Basic Qualifications:** * Bachelor's Degree OR * AA Degree and 2+ years' experience in biotechnology or related field and Quality Control experience OR * High School Degree and 3+ years' experience in biotechnology or related field and Quality Control experience **Preferred Qualifications:** * Strong knowledge of GMP, SOPs and quality control processes. * Identifying, writing, evaluating, and closing OOS's and investigations. * Proficient in MS Word, Excel, Power Point and other applications. * Strong written and verbal communication skills. * Ability to communicate and work independently with scientific/technical personnel. * Well versed in various analytical techniques such as Flow Cytometry, ELISAs, PCR, and cell bioassays and other applicable methods to the testing of biopharmaceuticals. * Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211). * Preferred: Experience in the biotech and/or pharmaceutical industry. * Quality Control Chemist * CRF Part 11 * Biotechnology * Pharma * Pharmaceuticals * quality * regulatory * 21 CRF Part 11 * Flow Cytometry * ELISAs * PCR * GMP * SOPs * Cell based bioassays * Flow Cytometry * ELISA * qPCR assays * Pharmaceutials **Privacy Overview** CookieDurationDescription

MacroGenics is a leader in the discovery and development of innovative medicines that utilize our next generation antibody-based technologies. Our team of 350+ dedicated individuals is advancing a pipeline of product candidates to treat patients with cancer. Our products and platforms have attracted multiple partnerships with leading pharmaceutical and biotechnology companies around the globe. MacroGenics is a bold, highly engaged, and diverse team driven by a passion for improving the lives of patients through innovative science. We are committed to an inclusive workplace built on trust and respect. We value and nurture strong connections with one another and foster collaborative relationships. We empower our people and drive personal accountability. We encourage curiosity and embrace our entrepreneurial spirit. We celebrate our successes and create a learning environment where all employees can thrive! Summary of Position This position is responsible for performing activities to support analytical testing programs at MacroGenics to ensure compliance with cGMP standards including in-process, product release and stability testing. This individual will guide and partner with lower level QC analysts to provide feedback and technical information. This individual will also ensure accurate documentation, timely completion of all analytical related testing, and timely review of data, while adhering to standard operating procedures and cGMPs. Responsibilities and Job Duties: * Performs routine analytical testing including complex methods such as ELISA, Bioassays, and Cell Culture as well as basic methods such as concentration by UV absorbance, pH, conductivity, and osmolality, for in-process, product release, and stability samples on a daily basis in accordance with all protocols and procedures. Enters data into Laboratory Information Management System (LIMS). * Perform cell culture for both adherent and suspension cells and independently plate/monitor and set up bioassays as needed. * Performs peer review of test data generated by other analysts to identify discrepancies and out of range results and to ensure adherence to standard operating procedures and GMPs. * Identifies analytical data trends and reports findings and provides recommendation to supervisors for review and consideration. * Conducts investigation when there are out of specification results from testing and reports to supervisor. * Initiates and monitors progress of analytical related Quality event records (e.g., Deviations and CAPAs) and conducts investigations to determine root cause and possible resolution. * Develops, revises, and updates standard operating procedures, as needed. * Collaborates with Development (Analytical Sciences) team members to participate in the development, transfer, and validation of analytical testing methods and conducts training on analytical test methods to other QC Analysts as needed. * Collaborates with partners and CDMOs for tech transfer and method validation as needed. * Oversees lab equipment calibration and maintenance processes as required for testing per standard operating procedures, and raises any concerns about equipment to supervisor for resolution. * Participates in troubleshooting of analytical test methods and instruments, as needed. * Performs special projects related to problems encountered with analytical testing and instruments, and makes recommendations for solutions that will minimize future issues. * Mentors and trains lower lever analysts, as needed. * Authors Reports, protocols as well as memos for validation, critical reagents and etc. * Keeps track of Critical Reagent inventory and current expiration dates Keeps track of failed samples, performs data reviews of failed samples as needed, helps review protocols, reports, create templates/overlays, creates SoftMax Templates and reviews SoftMax Templates. * Prepares general lab solutions and buffers as needed and monitors expirations of these solutions and buffers. * Orders reagents as needed. Qualifications QC Analyst III Education, Experience, & Credentials * Bachelor's Degree in a scientific discipline and minimum of 4 years experience in GMP environment * Experience in one or more of the following areas required: ELISA, Bioassays, Potency testing, Residuals, Quality Control, Raw Material testing, and/or GMP testing. Sr. QC Analyst Education, Experience, & Credentials * Bachelor's Degree in a scientific discipline and minimum of 6 years' experience in GMP environment * Experience in one or more of the following areas required: ELISA, Bioassays, Potency testing, Residuals, Quality Control, Raw Material testing, and/or GMP testing. Knowledge, Skills and Abilities * Working knowledge of good laboratory practices. * Excellent understanding of GMPs related to the biotech or pharmaceutical industry * Extensive experience in working different types of cell lines both adherent and suspension cells. * Working knowledge of aseptic technique * Experience in building, reviewing SoftMax Pro templates * Working knowledge of usage of cell counter, plate readers (M5, M2, L-reader) as well as Laboratory Information Systems. (LIMS). * Working knowledge of LIMS (Laboratory Information Management Systems ) * Working knowledge of SoftMax Pro, Prism and JMP. * Ability to organize and prioritize daily activities to meet internal customer needs in a fast-paced environment. * Ability to work on extremely complex problems in which analysis of situation or data requires an in‑depth evaluation of intangible variables. * Ability to act independently to determine methods and procedures on new assignments. * Demonstrate the confidence to exercise independent judgment in developing methods, techniques, and evaluation criteria for obtaining results. * Demonstrating ability to coach and train others. * Be able to work in a team environment in a cooperative and respectful manner. * Ability to stand for periods of time when performing tasks on the floor. * Ability to work a varied schedule including off shift and weekends. * Ability to lift up to 50 pounds. Supervisory Responsibilities None Additional Information The annual rate of pay for this position ranges from $78,700 to $122,100 (QC Analyst III) and $98,600 to $152,900 (Sr. Analyst). For non-exempt roles, and according to applicable regulations, there may be the possibility for overtime pay. This role is eligible for the Company's discretionary bonus and discretionary equity incentives. Eligible employees may participate in the Company's benefits programs, including medical / dental / vision / prescription coverage, employee wellness resources, 401(k) plan with employer match, access to an Employee Stock Purchase Plan, (ESPP), paid time off & paid parental leave benefits, and disability benefits. The annual pay rate range is described in good faith, and the Company believes is the range of possible compensation for this role at the time of this posting depending on the candidate's experience, qualifications, geographic location, and other factors permitted by law. The Company may ultimately pay more or less than the posted range, and this range may be modified in the future. No amount is considered to be wages or compensation until such amount is earned, vested, and determinable under the terms and conditions of the applicable policies and plans. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Statement MacroGenics is proud to be an equal opportunity employer. Employment selection and related decisions are made without regard to race, color, national origin, sex, gender identity, sexual orientation, religion, age, disability, protected veteran status, or any other characteristic protected by federal, state or local law. We are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please email ******************** or call ************** and/or 711 for TTD/TTY service. Equal Opportunity Employer/Veterans/Disabled We do not accept non-solicited resumes or candidate submittals from search/recruiting agencies.

Who We Are: CP&P is a valued supplier of precast concrete pipe and structures in the Mid-Atlantic and Southeast U.S. We take pride in delivering the best quality and value in precast concrete pipe products and solutions to our customers. Our people are the heart of our business. We highly value employee safety, but integrity, relationships, and mutual respect are equally important to us, and we hold ourselves accountable to our customers and our employees. CP&P is Not Just Concrete - Concrete Solutions! Position Snapshot: The QC Technician will inspect, test, sort, sample, or weigh raw materials or processed, machined, fabricated, or assembled products for defects. They may use precision measuring instruments and complex test equipment. Essential Functions and Responsibilities: Inspect products using gauges, coordinate measuring machine, scales, and vision prior to shipment. Generate spreadsheets for data collection. Reconcile final inspection documentation for shipments. Interact with Government Source Inspector as needed. Test incoming and finished product and raw materials. Operate, clean, and maintain batch plant. All other duties as assigned by the Plant Manager. Knowledge, Skills, and Abilities: Up to three (3) years of experience in Quality Control function in a concrete manufacturing environment. Ability to perform multiple tasks in a fast-paced environment to assure delivery requirements. Clear oral and written communication skills. Ability to keep accurate records. Ability to follow documented procedures and standards. Excellent time management skills, with the ability to work independently with little supervision. Knowledge of concrete batching design. Ability to frequently lift heavy objects. Ability to use hand tools, power tools, weighing and testing equipment. Qualifications: High school diploma or GED equivalent required. State-required concrete technician certification for the state of Maryland. ACI certification, or willingness to be trained for and achieve certification. Requirements: Must reside in the continental U.S. within the assigned region. No relocation assistance is provided. Must have a valid driver's license. Must be authorized to work in the U.S. for any employer. Typical Schedule: Work is generally performed Monday-Friday, 40+ hours per week depending on workload and production demands. Overtime and weekend work will be required during heavy production periods. Typical Physical Demands: Physical agility and may require any or all of the following: standing, sitting, walking, climbing, reaching, bending/stooping, lifting (50lbs. max), pushing/pulling (50lbs. max). Working Conditions: Work is performed in a production environment, with ambient weather/air conditions, loud noise, dangerous equipment, and variable lighting. Personal Protective Equipment (PPE) is required in all production and loading areas. Facility management to review complete inventory of SDSs prior to offering position. Compensation: Based on skills, knowledge, and experience Benefits: CP&P is proud to offer a comprehensive benefits package, including Health, Prescription, Dental, Vision, Life, Accidental Death & Dismemberment, Disability, FSA, 401(k), Legal & Identity Theft Protection, Accidental Injury, Critical Illness Insurance, Paid Holidays, Paid Time Off (PTO). CP&P provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Ubicación: Alcalá de Henares, MD, ES Equipo: Calidad Tipo de empleo: Permanente Puig es uno de los principales actores mundiales en la industria de la moda y la belleza. Contamos con un amplio porfolio de marcas de lujo globalmente reconocidas en moda, fragancias, maquillaje, cuidado de la piel y bienestar. Fundada hace más de 100 años, Puig es una empresa familiar que opera con responsabilidad con el entorno y la comunidad y con un firme compromiso a largo plazo hacia nuestras marcas y nuestros empleados. ****Mission**** To ensure the quality level of packaging materials, and finish products during materials incoming and filling process. ** **We'd love to meet you if you have**** **Education:** * Senior High School (Senior Technician in Quality, Production Technician or similar) * Other Technical studies will be valuable as any degree related to the Chemical Industry or similar **Languages:** * Medium level in English * French knowledge is also valuable **Shift Requirements:** * Work on three shift scheduled team is required **Personal skills:** * Highly adaptable person * Dynamism and flexibility * Team player, able to understand others stakes and to make win-win decisions * Productive work habits * Supplier relationship management * Experience in industry environment ** **What you'll get to do**** **Main functions and responsibilities:** * To control or audit samples of packaging materials and finish product * To carry out the release and refusal of packaging components and product * To ensure quality control plans follow up * To take care of quality level compliance within production staff * To participate in the non-conformity management process * To participate in the new reference process ensuring specification availability for production * To propose improvements over the process, products, or materials to increase the value of our operations inside a technological advanced system * To ensure the compliance of the GMP, instructions of health and security and environmental protection. * Una cultura de trabajo emprendedora, creativa y acogedora * Oportunidades de aprendizaje y desarrollo * Una empresa internacional con muchas oportunidades de crecimiento profesional * Un paquete competitivo de compensación y beneficios Puig ofrece igualdad de oportunidades y todos los solicitantes cualificados serán considerados por igual sin discriminación por razones de raza, color, religión, género, identidad de género, orientación sexual, origen nacional, etnia, edad, discapacidad, estado civil, estado de veterano o cualquier otra característica protegida por la ley. En Puig, buscamos personas entusiastas y comprometidas con una amplia gama de conocimientos y experiencias para unirse a nuestro equipo. Creemos que, creando un entorno inclusivo en el que te sientas bienvenido, valorado y empoderado, fortalece nuestro negocio y fomenta una cultura en la que todos nos sentimos inspirados a trabajar, innovar y a desafiarnos a nosotros mismos. Además, creemos que la diversidad de nuestros empleados nos convierte en una empresa más fuerte y más capaz de servir a nuestros clientes en todo el mundo. Job Req ID: 27438 *Puig 2024. This information is privileged, confidential and contains private information. Any reading, retention, distribution or copying of this communication by any person other than its intended recipient is prohibited.*

Description CookieYes sets this cookie to remember users' consent preferences so that their preferences are respected on subsequent visits to this site. It does not collect or store any personal information about the site visitors. Description This cookie is set by Hubspot whenever it changes the session cookie. The \_\_hssrc cookie set to 1 indicates that the user has restarted the browser, and if the cookie does not exist, it is assumed to be a new session. Description HubSpot sets this cookie to keep track of sessions and to determine if HubSpot should increment the session number and timestamps in the \_\_hstc cookie. Description The website's WordPress theme uses this cookie. It allows the website owner to implement or change the website's content in real-time. Description Cloudflare set the cookie to support Cloudflare Bot Management. Description Google Analytics sets this cookie to calculate visitor, session and campaign data and track site usage for the site's analytics report. The cookie stores information anonymously and assigns a randomly generated number to recognise unique visitors. Description Google Analytics sets this cookie to store information on how visitors use a website while also creating an analytics report of the website's performance. Some of the collected data includes the number of visitors, their source, and the pages they visit anonymously. Description Google Analytics sets this cookie to store a unique user ID. Description Hubspot set this main cookie for tracking visitors. It contains the domain, initial timestamp (first visit), last timestamp (last visit), current timestamp (this visit), and session number (increments for each subsequent session). Description HubSpot sets this cookie to keep track of the visitors to the website. This cookie is passed to HubSpot on form submission and used when deduplicating contacts. Description YouTube sets this cookie via embedded YouTube videos and registers anonymous statistical data. Description Google sets the cookie for advertising purposes; to limit the number of times the user sees an ad, to unwanted mute ads, and to measure the effectiveness of ads. Description Youtube sets this cookie to track the views of embedded videos on Youtube pages. Description YouTube sets this cookie to measure bandwidth, determining whether the user gets the new or old player interface. Description YouTube sets this cookie to store the user's video preferences using embedded YouTube videos. Description YouTube sets this cookie to register a unique ID to store data on what videos from YouTube the user has seen. Description YouTube sets this cookie to register a unique ID to store data on what videos from YouTube the user has seen. Description YouTube sets this cookie to store the user's video preferences using embedded YouTube videos. IEH Laboratories, a Leader in Food Safety, is now accepting applications for a Laboratory Analyst position at its facility in Laurel, MD. Ideal candidates will possess the following: - A BS or BA in the biological sciences or related field - Strong attention to detail - Proficiency with data entry and computer applications - Ability to multitask and work in a fast-paced environment - Strong written and verbal communication skills - Strong understanding of aseptic technique in the laboratory Laboratory Analyst duties include: analysis of food samples for pathogens via PCR and immunoassay, various microbe enumerations, data entry, laboratory reporting, quality control, media preparation, and other duties as assigned. This is a full-time position and is eligible for standard benefits after a brief waiting period. The schedule for this position is Tuesday to Saturday, from 7PM to 3AM. The laboratory operates weekends, so candidates must be willing to work occasional weekends. Due to exposure to various food allergens in the laboratory environment, applicants with moderate-to-severe food allergies are discouraged from applying. To apply for this position please access the company's job posting at: ***************************************************************** After navigating to the URL listed above, you will be asked to complete optional self-identification surveys and submit your cover letter, resume and references in a combined, single PDF. Equal Opportunity Employer M/F/V/D “Know Your Rights” Poster: *************************************************************************************************

If you find science, speed, and helping address serious infectious diseases exhilarating, you have come to the right place. Individually, we're skilled, driven, and confident risk-takers. Collectively we're collaborative and accomplished. We're SuperNovas! Together we use our unique experiences, cultures, and learnings to turn innovation into reality while maintaining the highest standards. We value balance, encourage growth, and recognize that you are our most important asset. Build your future with us while bringing innovative vaccines to the world. We have a place for you! Novavax, Inc (Nasdaq:NVAX) is a biotechnology committed to helping address serious infectious diseases globally through the discovery, development and delivery of innovative vaccines to patients around the world. We have more than a decade of experience contending with some of the world's most devastating diseases, and we are here to make a difference. Hard-won lessons and significant advances illustrate that our proven technology based on solid science tested by decades of research, has tremendous potential to make a substantial contribution to public health worldwide. The Quality Control Senior Analyst is responsible for day to day operations related to release and stability testing, maintaining QC cell culture lines, and writing SOPs, deviations, change controls and CAPAs as part of typical QC operations. Responsibilities include but are not limited to: Performs GMP release and stability testing in Quality Control Write technical reports and supporting documentation such as deviation, reports, testing protocols, and trend analyses Review of laboratory notebooks, protocols and reports Perform day to day activities for cell propagation used for QC release and stability assays. Participate in technology transfer, method qualification and validation Perform validations or transfers of analytical methods in accordance with applicable policies or guidelines Participate in internal assessments and regulatory audits as required Ensure that written records and work undertaken are performed in accordance with cGMP and company procedures Leading the lab in 5S and routine housekeeping activities Maintain effective communication with other relevant groups, including but not limited to Quality Assurance, Manufacturing and Analytical Development Other duties as assigned Minimum requirements: Minimum of a Bachelor's degree or equivalent in a scientific discipline Minimum 8 years of industry experience in a cGMP laboratory, preferably related to biopharmaceutical industry operations Hands on experience performing ELISA in a cGMP environment Hands on experience performing SDS-PAGE in a cGMP environment Working knowledge of Sf9 Insect Cell Culture Procedures and cell-based assays e.g. HS plaque and Rapid Titer assay GxP (regulatory relevant skills and knowledge) GLP/GCP/GMP required Excellent analytical skills and knowledge Strong troubleshooting skills for equipment and software Solid ability to work independently (minimum supervision) Ability to lead others, as needed Ability to effectively collaborate with others Excellent communications skills and be conversant in computer systems Excellent multi-tasking and organizational skills. Excels in time management Strong attention to detail Job holder should be a good understanding of relevant regulatory/industry standards and requirements The annual base salary (or hourly wage) for this position falls within the range of $78,250.00-$101,750.00. However, the actual base pay offered may vary based on several individualized factors, such as market location, job-related knowledge, skills, and experience. Novavax offers a base salary, annual bonus, equity grants, professional career development/growth opportunities, and a comprehensive benefits package including medical, dental, vision, Rx, STD, LTD, Life, Optional Life, 401(k) plan. Equal Opportunity Employer/Veterans/Disabled Novavax is an equal employment opportunity employer. Employment and advancement opportunities are available to all individuals on an at-will basis, regardless of their race, color, national origin, religion, ancestry, citizenship status, military or veteran status, sex, sexual orientation, gender identity or expression, age, marital status, family responsibilities, pregnancy, disability, genetic information, protective hairstyle, or any other characteristic protected by applicable federal, state, or local law.

Piper Companies is looking for a QA Associate-Operations & Documentation to join a clinical pharmaceuticals company located in Frederick, MD. Responsibilities of the QA Associate include:Complete communication with both internal and external vendors Create new SOPS and improve existing ones Deal with quality records through initiation, tracking, and closure (Ex: Deviations, Change Controls, CAPAs, Out of Specification records) Complete reviews of manufacturing batch records Qualifications for the QA Associate include:B. S with 2+ years of experience Associate or Bachelor's degree in the Scientific field Compensation for the QA Associate includes:Rate Range: $70,000 - $80,000 Per Year Comprehensive Benefit Package: Employee Medical/Dental/Vision Keywords: Quality Assurance, Quality Assurance Associate, Quality Assurance Analyst, SOP, Supplier Audits, MasterControl, Batch Records, Deviations, Change Controls, CAPAs, Out of Specification, OOS, Document Control #LI-AS1#LI-ONSITE