Risk & Control Analyst
Quality control analyst job in New York, NY
This role is located in New York City and will require a hybrid work schedule of at least 2 days in office per week.
This role is for Officer level candidates.
About the Bank
Sumitomo Mitsui Trust Bank, Limited was established through the merger of The Sumitomo Trust and Banking Co., Ltd with Chuo Mitsui Trust and Banking, Ltd. on April 1, 2012. We are one of the largest asset managers in Asia and number one among Japanese financial institutions by AUM. The Bank provides an assortment of financial solutions and manages a broad spectrum of financial products across its global branches.
Department Overview:
The Americas Division (“AD”) was established in the Sumitomo Mitsui Trust Bank, Limited, New York Branch) (“SMTBNY”) to perform corporate functions and supervise U.S. entities. Established under the AD are the “Global Banking Unit (“GBU”), Americas Division” and “Global Markets Unit (“GMU”), Americas Division” which performs business functions. The Operations Risk Management Department (“ORM”) identifies and evaluates operational risks to which the New York Branch (“the Branch”) is inherently exposed as well as enables appropriate mitigating actions. Operations Risk Management (“ORM”) establishes and maintains appropriate policies, procedures and the operational risk management framework that incorporates Operational Risk Assessments, Key Risk Indicators (“KRIs”), and an oversight process through Operational Risk Management Meeting. ORM is directly involved in all operational risk related projects, matters and issues.
Your Role Overview:
Risk and Control Analyst is accountable for engaging in the proactive identification, escalation, and timely mitigation of operational risks. Responsible for administering Operational Risk and Control Self-Assessment (RCSA) including Control Testing and Risk Register. Participates in the design, supervision, and implementation of an RCSA program to provide support in identifying, assessing, monitoring, and escalating the risk assessments performed by the First Line of the Bank.
The analyst is given broad exposure to all functions and business lines within the Americas Division and is expected to execute all aspects of the Operational Risk Management Framework through the 2
nd
line of defense oversight activities.
Your Duties and Responsibilities:
Coordinate and conduct Risk and Control Self-Assessment (“RCSA”).
Coordinate and conduct Vendor Risk Assessment, Model Risk Assessment, and Operational Risk Event (Business Continuity) Assessment.
Conduct analyses of risk data to identify trends and potential areas of concern.
Perform deep dives to assess the design and operational effectiveness of controls surrounding key technology and operations processes, and to identify remediation for gaps to mitigate risks.
Challenge risks within scenario analysis.
Maintain Risk Registers.
Contribute to the New Product Approval process.
Research regulatory changes and/or risk trends applicable to area(s) of coverage.
Assist in various Operational Risk related projects and initiatives.
Proactively contribute to the risk culture and overall awareness of operational risk and contribute to the creation and delivery of operational risk management training and/or workshop sessions.
Prepare operational risk reports, schedule meetings, takes notes, prepare minutes, and maintain files for ORM department.
Provide analysis and coordination for the ORM department.
Provide challenges on key indicators and material operational risks.
Identify emerging operational risks in the context of the regulatory and business operation environment and assure that measures are being taken to mitigate these risks.
Serve as a subject matter expert for operational risk and control assessments, and independently prepare a comprehensive report.
Facilitate accurate and appropriate reporting of operational risks to senior management.
Analyze operational risk data (losses, metrics, or assessment results) to identify areas of excessive risk and to ensure that mitigation efforts are having the desired effect(s).
Perform other duties and responsibilities as assigned by management.
Your Qualifications:
Bachelor's degree or equivalent.
A minimum of 4-5 years of prior operational risk management experience with a financial institution.
Integrative thinking skills, basic risk management knowledge, good organizational, communication and influencing skills.
Analytical and thorough approach to form defensible conclusions from risk assessments.
Able to present to and respond effectively to internal and external stakeholders.
Team-oriented with strong interpersonal skills, able to calmly manage conflict and pressure in a demanding, high-volume environment.
Able to be flexible and capable of prioritizing based on changing internal or external demands.
Good computer skills in Microsoft Office including Excel, Word, and PowerPoint.
Why you should join SuMi Trust:SuMi Trust embraces flexible ways of working when the business and role permits. We provide employees with a hybrid working model, allowing for in-office work and work from home. Our diverse and inclusive environment along with our global presence enables us to collaborate and communicate to meet our business needs. We believe that efficient teams need truth, loyalty, and a strong sense of purpose to balance risk and their targets. We make sustainable business decisions to improve our society and the world. We believe that each person brings a unique value that drives the business though their creativity and passion.
The Employee Benefits package includes: Paid Time Off, medical, HSA, vision, dental, FSA, 401(k), profit sharing, legal plan, cancer indemnity plan, disability insurance, life insurance, employee assistance program, commuter benefits, business travel accident, paid volunteer day, paid memberships, paid seminars, and tuition assistance.
We offer many socialization opportunities for wellness, financial wellbeing, runs/walks, team building, happy hours, and activities to support the Sustainable Developmental Goals.
Check out our LinkedIn for our employee experience: ***************************************
We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, disability status, protected veteran status or any other characteristic protected by law. SuMi Trust provides reasonable accommodations for employees and applicants with disabilities consistent with applicable law. If you need a reasonable accommodation during the application
Auto-ApplyQuality Co-Op (Spring 2026)
Quality control analyst job in New York, NY
Job Description
Employment Type: Intern
Division: Field Operations
Department: Quality
Salary Range: $23 - $28/hour
The Quality Intern supports the Quality department in implementing and monitoring quality management processes across multiple projects in various phases of construction. This role offers broad exposure to construction operations while working closely with Quality Program Managers to uphold and enhance project standards.
Responsibilities / Essential Functions
Participate in the quality program by attending meetings, performing inspections, and verifying materials.
Assist with coordination and content development for Quality pre-operational meetings.
Provide technical support on project sites, including interpreting contract drawings and submittals.
Develop an understanding of project schedules and critical path activities.
Collaborate with Quality Program Managers on initiatives such as drain assembly analysis, finish floor build-up analysis, and water intrusion control planning.
Perform other tasks as assigned by the team.
Key Skills
Excellent written and verbal communication skills.
Strong initiative and problem-solving abilities.
High attention to detail.
Effective time management with the ability to handle multiple responsibilities and meet deadlines.
Ability to work in a team environment with a primary focus on collaboration.
Required Experience
Pursuing a Bachelor's Degree in Construction Management, Engineering, or a related field (preferred).
Demonstrated interest in construction management and the construction industry.
PART TIME / ON-CALL Mastering QC Operator- New York
Quality control analyst job in New York, NY
Resillion is a strategic partner for quality assurance. We offer worldwide services on the field of quality technology, testing, conformity, interoperability and assurance, from initiation to launch - for the software system, cybersecurity, the device, digital products and media content. With a passion for quality, Resillion provides end-to-end solutions to support customers in their strategic digital initiatives and offers a holistic approach for both software and hardware. Via our office in Europe, the United Kingdom, the USA, India and China, we bring together more than 500 experts who are committed to success. We combine the best human and artificial intelligence (AI) on advanced solutions for quality technology in the liver. Resillion offers deep sector knowledge and works together with the world's leading companies in telecom, media, energy & utilities, health care, finance and consumer electronics. *****************
Job Description
Set up playback devices, QC bays and monitors/ scopes according to established specifications.
Verify correct format, aspect ratio, audio configuration and file metadata based on client specifications and previous title history.
Take accurate line count and video/ audio measurements using industry standard waveform scopes and audio meters.
Perform thorough mastering level quality control inspection noting any and all audio/ video impairments and anomalies.
Ensure reports are consistent and accurate across all previous versions of a given title, which may require tracking new anomalies back to original sources and other aspect ratios/ formats.
Troubleshoot any technical issues with playback of assigned jobs.
Provide additional information regarding a particular job or specific anomaly as needed.
May be required to perform other duties as needed (including, but not limited to: file transmission and data management, training other operators, client review sessions, etc.)
Qualifications
Solid understanding of a wide variety of film, video and audio impairments and their underlying causes.
Extensive experience with all SD and HD formats and timecode 2K, UHD and 4K and HDR-10 and Dolby Vision experience a huge plus.
Extensive experience with any and all file-based workflows (including, but not limited to Tiff, DPX, J2K, ProRes, IMF packages).
Solid Clipster proficiency including building. cp files and understanding of timeline output settings/ bin clip properties
Experience with ColorFront Transkoder for QC or Production a plus
Abilitiy to read and understand MaxFaLL and MaxCLL HDR reports.
Superior attention to detail and accuracy.
Ability to think in a logical and organized manner and work efficiently under tight deadlines with minimal supervision.
Strong computer, scientific, and organizational skills
Excellent communication (oral and written) and attention to detail
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Basic Minimum Qualifications
:
3 to 5 years' experience as a Mastering Quality Control operator, working in a professional Post Production facility or studio.
Authorization to work in the United States indefinitely without restriction or sponsorship.
Additional Information
Location: New York, NY
Employment Type: Part-Time- On as needed basis
Schedule: Swing Shift
Salary: $25.00-28.00
Per Hour
Senior Quality Control Analyst (NYC)
Quality control analyst job in New York, NY
Working days: Mon - Fri Working hours: 10am - 7pm We are looking to hire an experienced diamond professional to join our NYC Office. You will be responsible for quality controlling diamonds and gemstones as well as managing all incoming and outgoing shipments to and from the office.
The main goal is to ensure that diamonds come in and out of the NYC office in the shortest delay, while ensuring that all diamonds are up to quality standards.
About Nivoda
Nivoda's growth trajectory has skyrocketed over the past 12 months, and we continue to expand across new regions at an unprecedented pace. Our DNA centers on understanding our customers' needs and offering them a seamless experience. With a growing team based in major cities worldwide, including London, New York, Hong Kong, and Mumbai, Nivoda is becoming the go-to marketplace for the global jewelry industry.
We are bold, innovative, and relentless in our pursuit of excellence as we transform an industry steeped in tradition.
What you'll do
* Quality control diamonds and gemstones
* Receive consolidated shipments via courier partners
* Mark orders as received in the Nivoda system.
* Repack and send orders along to the next destination while updating the Nivoda system.
* Hand-deliver diamonds to local customers when necessary
* Collect diamonds from local suppliers, perform quality check and package and ship to the next destination.
* Create shipments using the Nivoda platform and send labels to suppliers to ensure timely delivery.
* Liaise with suppliers for shipments and forward invoices to the finance department.
* Assist customer support with queries related to shipping, order updates and urgent delivery requests.
* Assist in the smooth overall operation of the office.
* Support in managing the administrative work related to the office.
* Follow up with courier partners.
* Process returned diamond from our customers.
* Assist and advise other team members and management on the continuous improvement of all the processes of the local office.
What you'll need
* Must have 2+ years of hands on diamond/gemstone experience
* Must have experience in stock control of high value products.
* Logistics experience or familiarity with different courier services and tracking systems is useful
* Attention to detail is a must.
* Honesty, professionalism, and integrity are essential.
* Alignment with the Nivoda company values and culture.
What you'll get
* Opportunity to join a fast-growing company at an early stage
* Unlimited PTO
* Medical, dental and vision cover
Senior Quality Control Analyst (NYC)
Quality control analyst job in New York, NY
Working days: Mon - Fri
Working hours: 10am - 7pm
We are looking to hire an experienced diamond professional to join our NYC Office. You will be responsible for quality controlling diamonds and gemstones as well as managing all incoming and outgoing shipments to and from the office.
The main goal is to ensure that diamonds come in and out of the NYC office in the shortest delay, while ensuring that all diamonds are up to quality standards.
About Nivoda
Nivoda's growth trajectory has skyrocketed over the past 12 months, and we continue to expand across new regions at an unprecedented pace. Our DNA centers on understanding our customers' needs and offering them a seamless experience. With a growing team based in major cities worldwide, including London, New York, Hong Kong, and Mumbai, Nivoda is becoming the go-to marketplace for the global jewelry industry.
We are bold, innovative, and relentless in our pursuit of excellence as we transform an industry steeped in tradition.
What you'll do
Quality control diamonds and gemstones
Receive consolidated shipments via courier partners
Mark orders as received in the Nivoda system.
Repack and send orders along to the next destination while updating the Nivoda system.
Hand-deliver diamonds to local customers when necessary
Collect diamonds from local suppliers, perform quality check and package and ship to the next destination.
Create shipments using the Nivoda platform and send labels to suppliers to ensure timely delivery.
Liaise with suppliers for shipments and forward invoices to the finance department.
Assist customer support with queries related to shipping, order updates and urgent delivery requests.
Assist in the smooth overall operation of the office.
Support in managing the administrative work related to the office.
Follow up with courier partners.
Process returned diamond from our customers.
Assist and advise other team members and management on the continuous improvement of all the processes of the local office.
What you'll need
Must have 2+ years of hands on diamond/gemstone experience
Must have experience in stock control of high value products.
Logistics experience or familiarity with different courier services and tracking systems is useful
Attention to detail is a must.
Honesty, professionalism, and integrity are essential.
Alignment with the Nivoda company values and culture.
What you'll get
Opportunity to join a fast-growing company at an early stage
Unlimited PTO
Medical, dental and vision cover
Auto-ApplyBakery Quality Control Specialist
Quality control analyst job in Fort Lee, NJ
QC Technician oversees regulatory and quality compliance in bakeries, including QC monitoring and issue reporting. It also involves contributing to bakery R&D efforts, working with consultants to develop new products.
JOB DUTIES (include but are not limited to the following):
Monitor and support the implementation and maintenance of whole Quality Management System. Those programs are but not limited to: record keeping, allergen, pest control, temperature of coolers and freezers, pre-op, internal audit, and quality control.
Monitoring the daily QC activities to ensure they are performed to the published procedures and are properly documented.
Visit corporate and franchise stores to support and educate bakery teams/ kitchen managers.
Regulate quality control of each bakery.
Identification of any quality problems and recommend changes in quality standard where necessary.
Working with consultants on innovating new potential products for the brand.
Testing new recipes in the test kitchens.
Data entry using common computer database software (Excel, Access or equivalent).
QUALIFICATIONS & SKILLS:
Prior bakery experience is required, with preferred experience in bakery industry research and development.
Knowledge of baking various types of bread and baking and decorating cakes.
Associate Degree, or Bachelors degree, or equivalent years of work experience
3-5 years of combined experience in food or ingredients and manufacturing.
Knowledge of GMPs and HACCP.
Basic understanding of food production fundamentals
Proficiency in MS Office Products (Outlook, Word, Excel & PowerPoint) and basic computer skills.
Excellent verbal and written communication skills.
Ability to read and interpret procedure manuals and regulatory documents, and to write reports.
Ability to effectively present information and respond to questions from management level.
Demonstrate ability to manage and prioritize multiple tasks and demands working with minimum supervision.
Detail oriented, excellent record keeping and documentation skills
Employee Benefit
Health Insurance options: PPO Medical, Dental, Vision covered (Company 100% paid) *insurance starts on the very 1st date.
Life Insurance (Company 100% paid)
Flexible Time (starting time can vary everyday)
Short Term and Long-Term Disability Leave (short term 100% covered)
Lifestyle Allowance (up to net $70 per Month)
Cellphone reimbursement eligible
Employee Discounts (40% off company products & services)
401(k) 5% Match (no vesting period!) from Day 1
Paid Time Off (generous and increases by tier!): Max ceiling of 180 hours PTO (15 days) the 1st year and increases by tier.
Wellness Day: 40 Hours (Use it or Lose it System)
Paid Maternity Leave (paid 100% for 12 weeks)
Paid Secondary Caregiver Leave (up to 2 weeks)
Paid Creative Leave
Paid Holidays (11 days)
Educational Benefit
Employee Club Activities
& Much More!
Experience:
Baking: 2 years (Required)
Willingness to travel:
25% (Required)
QC Chemist III - DPI
Quality control analyst job in Hauppauge, NY
Job Title: Quality Control (QC) Chemist III
FLSA Classification: Full-Time, Exempt Professional
Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs)
Reports To: Quality Control Manager
Salary: $80,340 - $102,835
Purpose:
The job of the "Chemist" is simply described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes-specific testing group. The role may be further modified based upon individual education, training, experience or a combination of all three.
Generally, modifier designation with respect to experience for Chemist are as follows. However, combination of education, training, and special skills will determine the assignment of Level to a specific individual:
Scope:
The scope (content and statements) of this is designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent is to give a general scope of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position and provide basic performance expectations. The scope of the job may be modified with respect to the department, group, and on an individual assigned basis to a sometimes-specific testing group. Consideration of education, relevant training, and experience or a combination of all three may also result in further modification of the role.
Duties and Responsibilities
The general duties and responsibilities of the "Chemist" include but are not limited to the following:
Conduct routine testing or other analysis in a specific group or department setting.
Conduct advanced testing and/or critical testing, as required.
Operate specialized equipment or conduct specialized skill testing
Working knowledge of raw materials testing and release
Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP
Lead investigation activities.
Ensure compliance to all data integrity and cGMP practices, procedures, and expect
Ensure compliance with all good documentation practices.
Other duties and responsibilities as assigned by the Head of the Department or Section Head
Education and Experience
Bachelor's degree (BS or BA), physical sciences required
Master's degree preferred
Chemist III - minumum of 5 years' experience.
Proficiently speak English as a first or second language
Proficiently communicate and understand (read and write) scientific work in English
Have excellent organization, learning and teaching skills required to work in teams
Ability to understand and analyze complex data sets.
Working knowledge of Microsoft Office programs and other scientific based software.
Experience in Inhalation products (MDI) is a plus
Working conditions
This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required.
The role may be assigned on a work-shift basis, where required (Day, Evening, Night). Weekend or Holiday work may be requested or required.
Physical requirements
Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up-to10 kg, may be required.
Able to wear appropriate personal protective equipment at all times, when required.
Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period.
Professional and Behavioral Competencies
Must be willing to work in a pharmaceutical packaging setting.
Must be willing and able to work any assigned shift ranging from first or second shift. Work schedule may be Monday to Friday.
Must be willing to work some weekends based on business needs as required by management.
No remote work available
No employment sponsorship or work visas.
GLOBAL COMPANY
Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.
Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.
CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.)
About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited.
EEO Statement
Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.
QC Chemist III - DPI
Quality control analyst job in Hauppauge, NY
NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title: Quality Control (QC) Chemist III FLSA Classification: Full-Time, Exempt Professional
Work Location: Hauppauge, NY (Unit 1)
Work Hours: General Shift: 8:30AM - 5:00PM (may vary based on business needs)
Reports To: Quality Control Manager
Salary: $78,000 - $99,840
Purpose:
The job of the "Chemist" is simply described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department, group, etc., as exemplified in the "Department" on an individual assigned basis to a sometimes-specific testing group. The role may be further modified based upon individual education, training, experience or a combination of all three.
Generally, modifier designation with respect to experience for Chemist are as follows. However, combination of education, training, and special skills will determine the assignment of Level to a specific individual:
Scope:
The scope (content and statements) of this is designed to describe the general nature and level of work as well as provide a basic understanding of the role, responsibilities, and expectations of the person assigned to perform the job. This job description is not designed to provide an exact or exhaustive list of all job duties, tasks, skills, and qualifications. The intent is to give a general scope of the knowledge, skills, and abilities needed to satisfactorily perform the essential functions of the position and provide basic performance expectations. The scope of the job may be modified with respect to the department, group, and on an individual assigned basis to a sometimes-specific testing group. Consideration of education, relevant training, and experience or a combination of all three may also result in further modification of the role.
Duties and Responsibilities
The general duties and responsibilities of the "Chemist" include but are not limited to the following:
* Conduct routine testing or other analysis in a specific group or department setting.
* Conduct advanced testing and/or critical testing, as required.
* Operate specialized equipment or conduct specialized skill testing
* Working knowledge of raw materials testing and release
* Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP
* Lead investigation activities.
* Ensure compliance to all data integrity and cGMP practices, procedures, and expect
* Ensure compliance with all good documentation practices.
* Other duties and responsibilities as assigned by the Head of the Department or Section Head
Education and Experience
* Bachelor's degree (BS or BA), physical sciences required
* Master's degree preferred
* Chemist III - minumum of 5 years' experience.
* Proficiently speak English as a first or second language
* Proficiently communicate and understand (read and write) scientific work in English
* Have excellent organization, learning and teaching skills required to work in teams
* Ability to understand and analyze complex data sets.
* Working knowledge of Microsoft Office programs and other scientific based software.
* Experience in Inhalation products (DPI) is a plus
Working conditions
This role works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required, which may include uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc. Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required.
The role may be assigned on a work-shift basis, where required (Day, Evening, Night). Weekend or Holiday work may be requested or required.
Physical requirements
* Work standing or walking unassisted for 75% or greater of an 8-hour period. Unassisted lifting up-to10 kg, may be required.
* Able to wear appropriate personal protective equipment at all times, when required.
* Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period.
Professional and Behavioral Competencies
* Must be willing to work in a pharmaceutical packaging setting.
* Must be willing and able to work any assigned shift ranging from first or second shift. Work schedule may be Monday to Friday.
* Must be willing to work some weekends based on business needs as required by management.
* No remote work available
* No employment sponsorship or work visas.
GLOBAL COMPANY
Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world.
Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees, who lead us to prosperity and growth in the future. Driven by the vision, none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.
CIPLA NEW YORK (INVAGEN PHARMACEUTICALS, INC.)
About InvaGen Pharmaceuticals, a Cipla subsidiary InvaGen Pharmaceuticals, Inc. is engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. As of February 18, 2016, InvaGen Pharmaceuticals, Inc. operates as a subsidiary of Cipla (EU) Limited.
EEO Statement
Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.
Associate Quality Control Technician
Quality control analyst job in New York, NY
Disney Streaming is a business unit within The Walt Disney Company's Disney Entertainment and ESPN Technology (DEET) segment that oversees all consumer-facing digital video subscription services across the company. Disney Streaming is responsible for developing and operating The Walt Disney Company's direct-to-consumer video businesses globally, including the ESPN+ premium sports streaming service, programmed in conjunction with ESPN and the Disney+ service. Its core mission is to deliver global audiences the freedom to access content on their terms across any connected device, time or location.
We are seeking a talented, hard-working person for a part-time position in the Media Experience Department. We are seeking an experienced, dedicated Associate Quality Control Technician to join our team. In this position, you will maintain quality standards by approving incoming materials, in-process production, finished products, and recording the results. Excellent communication and leadership skills are a must, as well as a keen attention to detail.
Our environment is incredibly dynamic, fast-paced, and sophisticated. The ideal candidate has a background in video quality control and is extremely comfortable working in Mac OS X.
**Required Skills**
+ Understanding of mac OS and Windows operating system
+ Must be able to work a minimum of 28 hours per week
+ Must have an exemplary attention to detail.
+ Must possess strong communication skills.
+ Must possess solid organizational skills.
+ The candidate must be self-motivated.
+ The candidate must have a strong ability to multitask and adapt to new situations.
+ A solid computer and technical background, with experience working in new media and online organizations.
+ Familiarity with streaming and broadcast media
+ Familiarity with Google apps
+ Must be a team player, with an enthusiastic, congenial, and committed employee.
**Preferred Skills**
+ B.A. degree or equivalent
+ Fluency in languages other than English is a big plus particularly Arabic, Thai, Vietnamese, Czech, Slovak, Hungarian, Hebrew, Hindi, Malay & Indonesian.
+ Helpful skills include a background in encoding video for the web
+ An understanding of various video codecs, notably H.264
**Job Responsibilities**
+ Review and analyze video and audio files for visual and auditory defects (e.g., pixelation, audio sync issues, color correction errors).
+ Verify subtitles accuracy.
+ Log and document quality issues, generating QC reports and flagging critical errors for immediate attention.
The pay rate for this role in New York City is $24.5673 to $32.8846 per hour. The base pays actually offered may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience, among other factors. Select benefits may be provided as part of the compensation package, such as medical, financial, and/or other benefits, dependent on the level and position offered. To learn more about our benefits visit: ****************************************
**Job ID:** 10129066
**Location:** New York,New York
**Job Posting Company:** Disney Entertainment and ESPN Product & Technology
The Walt Disney Company and its Affiliated Companies are Equal Employment Opportunity employers and welcome all job seekers including individuals with disabilities and veterans with disabilities. If you have a disability and believe you need a reasonable accommodation in order to search for a job opening or apply for a position, email Candidate.Accommodations@Disney.com with your request. This email address is not for general employment inquiries or correspondence. We will only respond to those requests that are related to the accessibility of the online application system due to a disability.
Quality Control Specialist - Jewelry
Quality control analyst job in New York, NY
Job Description
R2Net is a diamond bridal jewelry company with a technology soul. R2Net Inc. is an innovative technology company that provides e-commerce and supply chain platforms to connect the entire span of the diamond industry's ecosystem, including manufacturers, retailers and consumers.
The QC Specialist will be responsible for performing the inspection of gemstones and jewelry items received from external vendors and from internal manufacturing. This role requires a keen eye for detail, extensive knowledge of marking requirements and craftsmanship, and the ability to work with precious metals and gemstones. The ideal candidate will have a strong background in jewelry, exceptional problem-solving skills, and a dedication to maintaining the highest standards of quality.
Responsibilities:
Responsible for performing inspection function ensuring all merchandise is in compliance with R2Net quality standards and legal requirements including functionality, stone setting, finish, hallmarking and trademarking. Report all critical fails to management.
Responsible for inspection of loose diamonds and colored gemstones for quality, authentication, and verification of all gemological documentation or electronic certificate. Report all critical fails to management.
Responsible for the accuracy of all new customer orders processed and the timely completion of the inspection.
Responsible for systematic movement of customer orders from QC admin receiving location to inspection workstation.
Responsible for completion of all daily work including current date orders and hard deadlines within area of responsibility.
Responsible for the processing of returns including the evaluation of the merchandise for quality and adherence to the terms of the return policy.
Maintain accurate records of quality control activities and inspection results.
Perform gemological testing and assist with special projects as needed.
Support QC operations for processing reverse logistics orders as needed.
Responsible for opening and closing activities for QC areas.
Requirements
3+ years of experience in jewelry repair and production preferred.
Graduate Gemologist degree preferred.
In-depth knowledge of industry standards and quality control inspection procedures.
Proficient in working with precious metals and gemstones.
Strong attention to detail and excellent hand-eye coordination.
Exceptional problem-solving skills and the ability to work under tight deadlines.
Capable of working independently as well as part of a team.
Excellent communication skills.
Working understanding of Microsoft office suite.
Benefits
At R2Net - James Allen & Blue Nile, many of our roles offer a high-quality, comprehensive benefits package including healthcare, paid time off, retirement planning and opportunities for career advancement. Some offerings are dependent upon the role, employment type, work schedule or location:
Hybrid Work Environment
Paid Time Off
Medical, Dental, Vision and Prescription Insurance
401(k) Retirement Plan with Company Match
Flexible Spending Account | Health Savings Account
Tuition Reimbursement
Employee Discount
Parental Leave
Life Insurance
Base hourly pay: $26-$32. Final pay rate shall be determined and is based on experience and qualifications.
At this time, R2Net will not sponsor a new applicant for employment authorization for this position.
Additional Information: R2NET INC. is an equal opportunity employer committed to diversity and inclusion in the workplace. All qualified applicants will receive consideration for employment without regard to sex (including pregnancy, childbirth or related medical conditions), race, color, age, national origin, religion, disability, genetic information, marital status, sexual orientation, gender identity, gender reassignment, citizenship, immigration status, protected veteran status or any other basis prohibited under applicable federal, state or local law. R2NET INC. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. #LI-WK1
Quality Control Inspector 1
Quality control analyst job in Newark, NJ
Are you detail-oriented and passionate about delivering high-quality products? At Hologic, we are seeking a Quality Control Inspector to ensure our products meet the highest standards of quality and compliance. In this role, you'll perform inspections, testing, and sampling procedures for manufacturing processes, packaging lines, and incoming materials. You'll play a key part in maintaining compliance with safety standards, supporting investigations, and driving continuous improvement initiatives. If you have a keen eye for detail, a commitment to excellence, and a desire to work in a collaborative environment, we'd love to hear from you!
Knowledge:
Familiarity with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
Basic understanding of quality control tools, including measuring tapes, calipers, micrometers, scales, gauges, and microscopes.
Knowledge of process auditing, documentation, and record-keeping.
Ability to read and interpret basic schematics and blueprints.
Awareness of FDA-regulated environments and medical device quality standards (preferred).
Skills:
Proficient in Microsoft Office applications, including Excel, Word, SharePoint, and OneDrive.
Strong verbal and written communication skills for accurate documentation and collaboration.
High attention to detail and focus on quality assurance processes.
Ability to follow written procedures and maintain accurate, organized records.
Capable of working both independently and collaboratively as part of a team.
Analytical mindset for supporting non-conformance investigations and identifying process improvements.
Behaviors:
Safety-conscious, maintaining a safe work environment and promptly addressing hazards.
Proactive and dependable, with a strong sense of accountability for quality and timelines.
Collaborative and team-oriented, fostering positive working relationships.
Adaptable and eager to contribute to continuous improvement initiatives like Kaizen events.
Reliable and punctual, with a commitment to maintaining attendance and meeting deadlines.
Experience:
0-1 years of experience in quality assurance or manufacturing roles, preferably in an FDA-regulated medical device environment.
Hands-on experience with quality control tools and techniques is beneficial.
Familiarity with clean rooms, controlled environments, and production processes is a plus.
Education:
High School Diploma (H.S./GED) required; an Associate Degree is a plus.
Why join Hologic?
We are committed to making Hologic the destination for top talent. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career.
The annualized base salary range for this role is $41,200-$61,800 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.
Agency and Third-Party Recruiter Notice
Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.
Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.
#LI-NT1
Auto-ApplyQuality Control Analytical Scientist
Quality control analyst job in Saddle Brook, NJ
Quality Control Analytical ScientistAllendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Devices industries in New Jersey. The QC Analytical Scientist will be a member of the Quality Control Department. As a Senior Member of the team the QC Analytical Scientist will be involved in various QC projects and should have a deep understanding of general QC flow and the Product Cycle.
Support internal and external customers to ensure that proper and timely execution of all aspects of the clinical analytical method life cycle across clients.
Support routine GMP testing as assigned. Mentor and train team members
Evaluate corporate and regulatory requirements along with coordination of activities for implementation of these requirements.
Write the contents of Analytical Method Transfer and Validation life cycle documentation including master plans, protocols, test methods, and reports.
Create validation project plan i.e., timelines and resources and provides status updates to management. Utilize statistical tools for evaluation of method validation and trending data.
Identify, evaluate, and implement continuous business process improvements.
Perform troubleshooting activities with respect to methods/assays, equipment malfunctions and investigations (Deviations and OOS).
Provide support during laboratory investigations.
Train QC personnel during method transfer and validation. Provide support during equipment qualification.
Consistently produce elevated level of documentation accuracy and clarity according to cGMP documentation practices.
Ability to set deadlines and prioritize work for self, group members, and support groups involved. Ability to review/approve work performed by coworkers for accuracy and alignment with procedures.
Indirectly may supervise cross functional teams including product development, QA, PMP, and Manufacturing.
REQUIREMENT
B.S Analytical Chemistry or other scientific field or MS/Ph.D. in Analytical Chemistry or other scientific field with demonstrated experience in Quality Control laboratories for biotechnology products.
8-10 years of experience in the areas of method development, validation, and transfer.
Direct GMP Experience.
Proficiency in project management skills and tools.
Strong background and in-depth knowledge in analytical chemistry e.g. Flow Cytometry, ELISA, HPLC, CE, PCR, etc.
Extensive knowledge and experience of QC assay development, transfer and validation, along with cGMPs.
Strong Quality orientation with attention to detail required. Analytical and problem-solving skills required.
Excellent communication skills, both written and verbal, with all levels of the organization, including the ability to state opinions clearly, ask questions, seek clarification, communicate facts objectively, challenge when appropriate, and pursue issues to resolution.
Excellent presentation skills. Ability to communicate to upper management, across departments and within the immediate QC team.
Ability to create and manage work plans and timelines and independently manage competing priorities with limited instruction.
Highly motivated individual with good interpersonal skills that have proven effective in managing relationships and negotiating solutions while maintaining a level of approachability with colleagues both internal and external.
Must be familiar with GMP lab environment and Aseptic techniques.
Working EnvironmentMust have the ability to work in a team-oriented environment and with clients Must be able to work during the weekend, holidays, or overtime and as required by the company May be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogen Must have the ability to work with specialized equipment Must be able to handle the standard/moderate noise of the manufacturing facility May work with hazardous materials and chemicals Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.
Chemistry Lab Technologist
Quality control analyst job in New York, NY
Our client is seeking Full -Time Clinical Lab Technologists for their Chemistry Lab! Full time - Alternate Weekends 11:30 pm - 8:00 am 10% night shift differential!!
Perform routine and emergency tests on blood and other body fluids using a variety of automated and manual instrumentation promptly.
Maintain equipment and records according to department procedures and regulatory agencies guidelines in the areas of QA and QC.
Use independent judgment to solve technical and procedural problems.
In some instances, the ability to stand or sit for extended periods of time is necessary.
Pay Range based on experience: $82,979.96 - $103,286.06
Requirements
Must have an active New York license
At least 2 years of work experience preferred Bachelor's Degree in physical science, medical technology preferred.
Benefits
1199 Members Medical & Dental
403B matching up to 8% of salary Room for Growth
Great leadership and support, utilizing the latest advances in computer technology.
Quality Control (QC) Assistant
Quality control analyst job in Teterboro, NJ
Northern Architectural Systems (“NAS”) is a growth-minded, locally owned and operated company which is dedicated to servicing our customers. We offer high quality, energy-efficient fenestration and building facade solutions to meet the requirements of a demanding market, while remaining environmentally-friendly. Northern Architectural Systems has been recognized by INC Magazine on the list of the top 5000 Fastest Growing Private Companies in America and as one of the top 50 Fasted Growing Companies in New Jersey by NJBIZ Magazine
Overview:
We are looking to fulfill our need for a Quality Control (QC) Assistant at our Teterboro, NJ facility.
Full-time position: Hours 7 am - 3:30 pm (Monday - Friday) Overtime when needed.
Applicants from NJ with their own reliable transportation preferred.
Requirements
Essential Duties and Responsibilities (other duties may be assigned):
Must be willing and eager to learn.
Learn how to check received product/raw materials.
Learn how to inspect manufactured products which includes final inspection of finished products prior to shipping.
Assist with product testing.
Create and build wooden buks to test our products.
Assist with the installation of our product into the buks for testing purposes.
Able to learn and become familiar with NAS's various product models.
Must be hands-on and a hard worker.
Maintain a clean, safe work environment.
Able to work in extreme temperatures.
Comfortable working in a diverse environment.
Must have the following skills:
No degree necessary (high school diploma or equivalent preferred)
Growth Opportunity
Operate Power Tools (power drill, power saw, etc.) a plus
Able to use a level and a square a plus
The ability to lift 50+ lbs.
Attention to detail and well organized
Blueprint reading a plus
Benefits
Full-time position
Hourly Rate Range: $18.00 - $23.00/hour
Medical, dental and vision benefits offered
401(k) Offered
PTO (Paid Time Off)
Employee Training
Auto-ApplyPer Diem Chemistry Laboratory Technologist
Quality control analyst job in New York, NY
Medical Laboratory Technologist to work in the Chemistry/Core Laboratory under the direct supervision of supervisor. Will be responsible for performing a variety of complex and routine test within the Core Laboratory complying with all safety and regulatory requirement. Rotate weekends and scheduled holidays base on the needs of the department; participate in interdepartmental collaboration within the institution, to provide the highest quality patient care.
Part-Time Lab Technician - Chemistry - Farmingdale State College
Quality control analyst job in Farmingdale, NY
The Chemistry Department at Farmingdale State College is seeking to fill a part-time Lab Technician vacancy for its academic laboratory program. * Assembly and disassembly of laboratory setups * Monitoring of a laboratory class, in conjunction with a faculty member, to ensure adherence to procedures,
* laboratory safety, and waste disposal
* Preparation of materials for laboratory sections
* Maintaining general safety and cleanliness of laboratory rooms
This position will require learning the laboratory preparations and assisting in laboratory observation for the Department's one year general chemistry course as well as the one-semester general and organic chemistry courses.
Work schedule would consist of day and evening hours for a total of 15-20 hours per week.
The college particularly welcomes candidates with knowledge, skills and abilities that include:
* Commitment to diversity and university initiatives supportive of diversity and inclusion.
* Interest in participating in student-centered service activities.
* Desire to apply expertise in promoting civic engagement with the College's many community partners.
Requirements:
MINIMUM REQUIRED QUALIFICATIONS:
* BS in Chemistry or a related field
* Minimum of 2 years experience in a laboratory environment
Additional Information:
This is a part-time, temporary UUP position.
* SALARY: $23.33/hour
The State University of New York offers excellent fringe benefits including health insurance options and retirement plans.
Click here for New York State PT UUP Benefits Summary
Visit our Why Work at FSC page to learn more about FSC and the total rewards we offer.
VISA SPONSORSHIP IS NOT AVAILABLE FOR THIS POSITION
The Consumer Information web page can be viewed at the following link
***********************************************************
This page describes various services, information and statistics on many different aspects of the College's operations.
Farmingdale State College's commitment to inclusive excellence is an important part of our mission of public education and our culture. At Farmingdale State College, we continue to work on building a community that supports freedom, mutual respect, and civility. We seek others who support these values of diversity and inclusiveness and candidates of all diverse backgrounds who wish to participate in our cultural aspirations are welcome and encouraged to apply.
The College is an Equal Opportunity/Affirmative Action employer and does not discriminate on the basis of race, color, national origin, religion, creed, age, disability, sex, gender identity, sexual orientation, familial status, pregnancy, predisposing genetic characteristics, military status, domestic violence victim status or any other legally protected
status.
Application Instructions:
Interested candidates may apply by clicking on the "Apply Now" link at the top or bottom of this page. The following documents are required for all positions:
* Cover Letter
* Resume/C.V.
Only applications made through Farmingdale's electronic application system will be accepted. Once you successfully apply you will receive an email as confirmation. Returning applicants may login to their Farmingdale State College Careers Account to apply for this position. See the FAQ for using our online system. Please contact us if you need assistance applying through this website.
Quality Co-Op (Spring 2026)
Quality control analyst job in New York, NY
Employment Type: Intern Division: Field Operations Department: Quality Salary Range: $23 - $28/hour The Quality Intern supports the Quality department in implementing and monitoring quality management processes across multiple projects in various phases of construction. This role offers broad exposure to construction operations while working closely with Quality Program Managers to uphold and enhance project standards.
Responsibilities / Essential Functions
* Participate in the quality program by attending meetings, performing inspections, and verifying materials.
* Assist with coordination and content development for Quality pre-operational meetings.
* Provide technical support on project sites, including interpreting contract drawings and submittals.
* Develop an understanding of project schedules and critical path activities.
* Collaborate with Quality Program Managers on initiatives such as drain assembly analysis, finish floor build-up analysis, and water intrusion control planning.
* Perform other tasks as assigned by the team.
Key Skills
* Excellent written and verbal communication skills.
* Strong initiative and problem-solving abilities.
* High attention to detail.
* Effective time management with the ability to handle multiple responsibilities and meet deadlines.
* Ability to work in a team environment with a primary focus on collaboration.
Required Experience
* Pursuing a Bachelor's Degree in Construction Management, Engineering, or a related field (preferred).
* Demonstrated interest in construction management and the construction industry.
Senior Quality Control Analyst (NYC)
Quality control analyst job in New York, NY
Job Description
Working days: Mon - Fri
Working hours: 10am - 7pm
We are looking to hire an experienced diamond professional to join our NYC Office. You will be responsible for quality controlling diamonds and gemstones as well as managing all incoming and outgoing shipments to and from the office.
The main goal is to ensure that diamonds come in and out of the NYC office in the shortest delay, while ensuring that all diamonds are up to quality standards.
About Nivoda
Nivoda's growth trajectory has skyrocketed over the past 12 months, and we continue to expand across new regions at an unprecedented pace. Our DNA centers on understanding our customers' needs and offering them a seamless experience. With a growing team based in major cities worldwide, including London, New York, Hong Kong, and Mumbai, Nivoda is becoming the go-to marketplace for the global jewelry industry.
We are bold, innovative, and relentless in our pursuit of excellence as we transform an industry steeped in tradition.
What you'll do
Quality control diamonds and gemstones
Receive consolidated shipments via courier partners
Mark orders as received in the Nivoda system.
Repack and send orders along to the next destination while updating the Nivoda system.
Hand-deliver diamonds to local customers when necessary
Collect diamonds from local suppliers, perform quality check and package and ship to the next destination.
Create shipments using the Nivoda platform and send labels to suppliers to ensure timely delivery.
Liaise with suppliers for shipments and forward invoices to the finance department.
Assist customer support with queries related to shipping, order updates and urgent delivery requests.
Assist in the smooth overall operation of the office.
Support in managing the administrative work related to the office.
Follow up with courier partners.
Process returned diamond from our customers.
Assist and advise other team members and management on the continuous improvement of all the processes of the local office.
What you'll need
Must have 2+ years of hands on diamond/gemstone experience
Must have experience in stock control of high value products.
Logistics experience or familiarity with different courier services and tracking systems is useful
Attention to detail is a must.
Honesty, professionalism, and integrity are essential.
Alignment with the Nivoda company values and culture.
What you'll get
Opportunity to join a fast-growing company at an early stage
Unlimited PTO
Medical, dental and vision cover
Mastering QC Operator - Swing Shift
Quality control analyst job in New York, NY
Resillion US, LLC. is a leading content QC company that works with major streaming services and entertainment platforms to bring diverse stories to a global audience. We value precision, inclusivity, and creativity in delivering the best viewing experience to subscribers all around the world.
One of our specialties focused on preserving and revitalizing iconic content for audiences around the world. We are passionate about blending artistry with state-of-the-art technology to restore classic films, television shows, and media to their original brilliance while enhancing them for modern viewing standards. Our high-profile projects celebrate the history of entertainment and push the boundaries of digital restoration.
Job Description
Set up playback devices, QC bays, and monitors/ scopes according to established specifications.
Verify correct format, aspect ratio, audio configuration, and file metadata based on client specifications and previous title history.
Take accurate line count and video/ audio measurements using industry standard waveform scopes and audio meters.
Perform thorough mastering level quality control inspection noting any and all audio/ video impairments and anomalies.
Ensure reports are consistent and accurate across all previous versions of a given title, which may require tracking new anomalies back to original sources and other aspect ratios/ formats.
Troubleshoot any technical issues with playback of assigned jobs.
Provide additional information regarding a particular job or specific anomaly as needed.
May be required to perform other duties as needed (including, but not limited to: file transmission and data management, training other operators, client review sessions, etc.)
The ideal candidate would possess
:
Solid understanding of a wide variety of film, video and audio impairments and their underlying causes.
Extensive experience with all SD and HD formats and timecode 2K, UHD and 4K and HDR-10 and Dolby Vision experience a huge plus.
Extensive experience with any and all file-based workflows (including, but not limited to Tiff, DPX, J2K, ProRes, IMF packages).
Solid DaVinci Resolve proficiency, including building files and understanding of timeline output settings/ bin clip properties
Experience with ColorFront Transkoder for QC or Production a plus
Abilitiy to read and understand MaxFaLL and MaxCLL HDR reports.
Superior attention to detail and accuracy.
Ability to think in a logical and organized manner and work efficiently under tight deadlines with minimal supervision.
Strong computer, scientific, and organizational skills
Excellent communication (oral and written) and attention to detail
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Salary Range $25.00-27.00 Per Hour
Qualifications
3 to 5 years experience as a Mastering Quality Control operator, working in a professional Post Production facility or studio.
Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information
Equal Employment Opportunity -
Resillion US, LLC is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race, color, religious creed, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth and related medical conditions), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, protected medical condition as defined by applicable state or local law (such as cancer), genetic information, or any other characteristic protected by applicable federal, state or local laws and ordinances. Resillion US, LLC management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities, access to facilities and programs and general treatment during employment. All your information will be kept confidential according to EEO guidelines.
Disclaimers
Headhunters and recruitment agencies may not submit resumes/CVs through this website or directly to managers. Resillion does not accept unsolicited headhunter and agency resumes and will not pay fees to any third-party agency.
In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.
All offers of employment at Resillion US, LLC. are contingent upon clear results of a thorough background check.
QC Chemist I
Quality control analyst job in Central Islip, NY
NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title QC Chemist I Organization Name InvaGen Pharmaceuticals, Inc.
Employment Type
Full Time - Salary/Exempt
Benefits
In addition to a fulfilling career and competitive salary, the Company offers a comprehensive benefits package to include a 401(k) savings plan and matching, health insurance - medical/dental/vision, health savings account (HSA), flexible spending account (FSA), paid time off (PTO) - vacation/sick/flex time, paid holidays, short-term disability (STD), long-term disability (LTD), parental leave, paid and unpaid family leave, employee discounts, and other benefits.
Work Hours/ Shift/ Remote
8:30 AM - 5:00 PM (General Shift)
Salary Range
$62,400 - $75,400
Responsibilities/ Accountabilities
* Demonstrated ability to perform independent work requiring attention to detail, accuracy and scientific judgment and a consistent record of shifting thought processes quickly from one task to another.
* Strong analytical skills, attention to detail, knowledge of analytical techniques (HPLC, GC, UV-Vis etc.) and familiarity with quality control procedures.
* Responsible for performing routine analytical testing of raw material, in-process samples, finished products to ensure they meet quality standards and regulatory requirements.
* Understanding of regulatory compliance, quality management systems and document control processes, and the ability to collaborate cross-functionally and communicate effectively.
* Responsible for QA review and approval of the following types of documents:
* SOP's
* GMP documents
* Change control documents
* Review of system records
* Perform activities related to periodic audit trail review of all quality softwares, ensure compliance within the systems etc.
* Maintaining regulatory compliance in accordance with cGMP and Perform Data Integrity risk assessment of current Good Manufacturing Practices (cGMP) and GLP systems both manual and automated.
* Follow all safety procedures and guidelines to ensure a safe laboratory environment.
* Prioritize risks and work with IT, QA, laboratory personnel to mitigate data integrity gaps.
* Partnering with other members of the Quality Assurance team and/or end users of the system to Identify, Develop, and Implement Continuous Improvements to the Change Control System, Process, and associated procedures.
* Evaluate proposed and existing software systems that support laboratory and software applications for data integrity gaps. Works with IT and QA to resolve those gaps.
* Develop standard operating procedures for the administration of analytical and QC equipment.
* Ensuring the GMP status and the functionality of the laboratory equipment in accordance with the guidelines 21 CRF Part 11 on data integrity.
* Excellent written and verbal communication skills.
* Perform additional duties as requested.
Education Qualifications/Experience
* Entry level position.
* Master's degree in chemistry, pharmaceutical or related field is required.
* May require 1+ years' experience in a pharmaceutical manufacturing lab.
* Experience and understanding of the Laboratory Information Management Systems (LIMS) is a plus.
* Understanding of systems such as polarimeter, IR spectroscopy, Karl Fischer etc. is expected.
* Proficient digital literacy in Microsoft (MS) Word, Excel, PowerPoint, and SharePoint required.
* Experience in Chromatographic softwares such as Empower3, Chromeleon preferred. Understanding or experience in other quality systems such as Trackwise, master control is a plus.
About Cipla
Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded, and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades, we have strengthened our leadership in India's pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India, South Africa, the U.S., and other economies of the emerging world. Driven by the purpose 'Caring for Life', Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world. In the last 85 + years, Cipla has emerged as one of the most respected pharmaceutical names in India as well as across more than 100 countries. Cipla is a fast-growing pharmaceutical company with a continued focus on the expanse of our strong legacy. Over the last five years, Cipla has significantly expanded its portfolio and presence in the U.S. with both a generic and brand division.
InvaGen Pharmaceuticals, Inc.
InvaGen Pharmaceuticals is a Cipla subsidiary engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on a range of therapeutic areas, including cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge, New York. In October 2020, InvaGen established its project site in Fall River, Massachusetts to support the launch of Cipla's respiratory business in the United States.
Equal Opportunity Employer
Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require reasonable accommodation to make your application or interview experience a great one, please contact the recruiter.
About the Salary/ Pay Range: The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.