Manufacturing associate jobs in Fall River, MA

Pay: Up to $34/hour (differentials for weekend) Shift: We are hiring for nights. Role: (Contract) Manufacturing Associate I Duration: Six-month contract (with possible extension) Required Experience: Bachelor's Degree in a related field OR Associate's Degree with 2+ years of experience OR 4+ years of related GMP experience We are seeking a Manufacturing Associate I to join a cohesive team at a state-of-the-art GMP Manufacturing site in Norwood, MA. In this role, you will play a key part in producing mRNA-based medicines for clinical trials. If you're detail-oriented, thrive in a fast-paced environment, and want to contribute to innovative healthcare solutions, this is the opportunity for you! Responsibilities Operate manufacturing equipment and execute processes to produce mRNA medicines Use disposable technologies, automation systems, and Manufacturing Execution Systems (MES) Work closely with Quality Assurance (QA) to ensure rapid product release Follow Good Manufacturing Practices (cGMPs) and Standard Operating Procedures (SOPs) Document equipment operations and process steps clearly and accurately Monitor production processes to ensure compliance with quality standards Support investigations into any deviations or issues that arise during production Maintain a clean, safe, and compliant work environment (including gowning procedures) Practice safe work habits and follow site safety guidelines Look for opportunities to improve operational efficiency Qualifications Biotech Laboratory/Sciences GMP Experience Experienced 4 year(s)

About the 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. About the Role The purpose of this role is to assist in packaging manufactured metered dose inhalation (MDI) products in a pharmaceutical manufacturing company. Responsibilities Understanding basics of mechanical machinery and principles of control systems. Operating pharmaceutical packaging equipment with minimum rejection and maximum output maintaining quality standard within standard norms. Cleaning machines and area as per batch to batch and product to product change over. Performing operations and preventative maintenance of machines. Identifying and assisting in the corrective actions of packaging related issues. Correcting status labelling at all stages of packing line with signature. Ensuring that appropriate equipment calibrations are performed, and records are maintained. Ensuring line clearance before initiating packaging activities in each area. Wearing appropriate PPE as stated in the SOP before initiating process. Working individually and in collaboration with others as part of a team. Executing procedures to complete tasks in a safe and efficient manner. Completing documents on time, ensuring accuracy and completeness. Adhering to all cGMPs, compliance/regulatory mandates and quality requirements. Complying with company policies and procedures. Performing duties through the proper safe use of equipment, according to Health & Safety procedures and Equipment Manuals. Performing other related duties as assigned. Qualifications High school diploma or equivalent is required. Accredited college certificate or university degree is preferred. Minimum of one (1) year experience in packaging operations preferred. Proficient in the English language (Speaking/Reading/Writing) to understand work instructions and document results. Knowledge of fundamental cGMP and regulatory requirements in a pharmaceutical manufacturing environment highly preferred. Basic understanding of mechanical machinery and the operating principles of control systems. Ability to follow both verbal and written instructions. Demonstrated ability to work in both independent and team environments. Good knowledge of Health & Safety procedures, including, OSHA. Strong mathematical and organizational skills. Required Skills Minimum of one (1) year of experience working in a pharmaceutical, nutraceutical, cosmetic or other cGMP environment. Hands-on experience with current Good Manufacturing Practices (cGMP) and following Standard Operating Procedures (SOPs). Experience in wearing and working with Personal Protective Equipment (PPE). Preferred Skills Good Documentation skills (writing and reading batch records). Good knowledge of Health & Safety procedures, including OSHA. Pay range and compensation package Salary: USD 39000 - 41000 Compensation Details: Salary Maximum: $19/hr - $20/hr Equal Opportunity Statement We are committed to diversity and inclusivity.

Manufacturing Test Technician 6 months contract (with possibility of extension) Westborough, MA (onsite) Pay Range: $25/h - $35/h on W2, DOE We are looking for a technician for 6 months that can come in and support an Engineer developing a manufacturing test process for a Mechatronics machine that inducts and labels packages. This test solution will be focused on Control Panels, conveyance, printers, dimensioners, weigh scale, delta robot labeler and vision systems. This is an electromechanical product with high PLC and IO content. The tech will aid the engineer to create and integrate the test solutions that will eventually be shipped to a contract manufacturer. This is a hands-on role. The expectation is the tech can be self-motivated and translate direction from the Engineer into actions and deliverables. The tech will support setting up the systems and the environment to test products and integrate the test solutions. The technician will need to be able to travel to local suppliers for custom test panels or other solutions to perform acceptance testing per the direction of the lead engineer. Required: Basic mechanical aptitude for test system installation and assembly. Proficiency in electrical wiring, routing, and connections. Experience in electrical system troubleshooting and debugging. Ability to follow Standard Operating Procedures (SOPs) for system startup. Capable of executing test plans and procedures with minimal supervision. Knowledge of reading schematics and wiring diagrams. Experience in creating Bills of Materials (BOM) from technical documentation. Understanding of proper packaging and shipping procedures. Valid driver's license and ability to travel locally to vendor locations. Attention to detail and strong documentation skills. Ability to work independently and follow written/verbal instructions. Experience with quality control and testing procedures. Must be comfortable with hands-on technical work. Education/Experience: Technical degree or equivalent experience in electronics/mechanical field. 2+ years of experience in a similar technical role preferred. Certification in electronics or related field is a plus. Top 3 skills required: Proficiency in electrical wiring, routing, and connections. Experience in creating Bills of Materials (BOM) from technical documentation. Basic mechanical aptitude for test system installation and assembly. Russell Tobin offers eligible employee's comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), 401(k)-retirement savings, life & disability insurance, an employee assistance program, legal support, auto, home insurance, pet insurance and employee discounts with preferred vendors.

Job Title: Manufacturing Technician I (Quincy Plant) Job Title: Mfg. Technician Department / Division: Quincy Plant / Manufacturing Paygrade: NXA09 Hourly Rate: $23.28/hour What do we need: We are looking for a Manufacturing Technician to join our Quincy Plant. What's special about this job: The Quincy Plant is responsible for the extraction and concentration of nutrients for our Nutrilite Brand. The Quincy plant runs 24-hours a day, six days a week. Shift schedules are from 4:00am to 4:30pm, or 4:00pm to 4:30am. This role would have a shift schedule of 36-hours a week, Monday - Wednesday and Thursday - Saturday, rotating every ten weeks. As a Manufacturing Technician in the plant, you will be part of a collaborative team, learning all aspects of the plant's operations. This role will have a focused career progression with a skill development system that allows for multiple avenues to promotion. How you would contribute to the role: In this role, you will be primarily responsible for learning and operating equipment used to process liquid concentrate into dried intermediate product. The plant handles the extraction and concentration process - from prepping the product, to running the extraction and concentration equipment, to inline QA testing, to cleaning and sanitization of all the equipment. Since this is a GMP regulated plant, it will be important to complete and maintain all required records and documentation. As you develop in your career, you will train other team members on proper standards and operating procedures and participate in continuous improvement. Required qualifications: * High School diploma * Ability to lift and carry 50 lbs. * Prior experience with manufacturing food products, troubleshooting and repairing manufacturing equipment, or working in cGMP environment is a plus Skills to be successful in the role: * Strong attention to detail/safety with a high level of accuracy, organizational, and time management skills * Ability to trust and follow through on commitments with team members * Drive to understand the root cause of issues, and develop and enhance processes * Willingness to adapt to different approaches, ideas, tools, techniques, and processes Amway does not provide immigration-related sponsorship for this role. Do not apply for this role if you will need Amway immigration sponsorship (e.g., H-1B, STEM OPT, TN, etc.) now or in the future. Apply now Information at a Glance Helping People Live Better Lives Amway is based in Ada, Michigan, U.S.A., with global headquarters still located on the same property where the company was founded. Family-owned and guided by enduring values, we continue to be shaped by our Founders Fundamentals. Since 1959, our heart has remained the same: helping people realize their potential. Today, that mission spans six continents and more than 100 countries and territories.

Since its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and rare diseases. The Nobel Prize-winning CRISPR science has revolutionized biomedical research and represents a powerful, clinically validated approach with the potential to create a new class of potentially transformative medicines. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic partnerships with leading companies including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California. Position Summary Reporting to the Manufacturing Sr Manager, the Manufacturing Associate will perform manufacturing activities associated with LNP GMP manufacturing within a state-of-the-art manufacturing facility at 33 New York Ave in Framingham, MA. A successful candidate will be responsible for the manufacture of LNP therapies for clinical studies and as a commercial product. This role requires clear communication across multiple departments for the execution of daily activities. The ideal candidate will have experience successfully performing formulated LNP Manufacturing within a GMP environment. Responsibilities * Perform clinical / commercial product manufacturing for LNP therapies according to cGMP standards and SOPs including Lipid and RNA Prep, T-Mix, and TFF operations * Perform aseptic vial filling, visual inspection, cryopreservation, process reagent formulation, and material kitting. * Transfer raw material inside cleanroom suite using sanitizing reagents or equipment. * Participates in technology transfer from Process Development to the Manufacturing group. * Assist in the life cycle development of Standard Operating Procedures (SOPs) for manufacturing in collaboration with PD / MSAT and Quality Systems groups. * Ensures all materials and equipment are identified and available in time for manufacturing operations. * Execute standard work per manufacturing schedule * Participate in Quality investigations and resolutions. * Ensure cGMP compliance through consistent execution. * Other duties and projects as assigned to meet departmental requirements. Minimum Qualifications * Certificate, associate's degree or higher in biological sciences or related fields and 2-5 years of relevant Manufacturing experience or related fields * Available to work a flexible schedule as needed. * Ability to don cleanroom garments and work within a classified environment (Grade B and C) * Knowledge of GMP and industry standards * T-Mix and TFF experience preferred * Fluency in Windows and Microsoft Office applications * Attentive to detail and accuracy * Ability to effectively communicate and collaborate with internal stakeholders is essential * Ability to work effectively in a collaborative team environment where results are achieved through influence and the incorporation of multiple points of view. Ability to execute and follow-through to completion * Ability to lift 40 pounds * Ability to stand for 6 hours in a clean room environment * Self-driven, independently motivated, data driven and excellent problem-solving ability Competencies * Collaborative - Openness, One Team * Undaunted - Fearless, Can-do attitude * Results Orientation - Delivering progress toward our mission. Sense of urgency in solving problems. * Entrepreneurial Spirit - Proactive. Ownership mindset. Due to the nature of their work, our manufacturing and lab-based positions are located fully on-site. Manufacturing Associate: Base pay range of $40.00 per hour to $44.00 per hour + bonus, equity and benefits. The range provided is CRISPR Therapeutics' reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities. CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. To view our Privacy Statement, please click the following link: ***********************************************

About this opportunity : As a Manufacturing Technician III, you'll be responsible for the implementation of assigned production operations working within defined production schedules in a cGMP environment. Key Responsibilities: May specialize in either purification or synthesis processes. As required, may cross train on basic or non-technical operations associated with other functions within the company. Maintain a clean and organized work environment in accordance with defined procedures. Assist Process Support Group in the execution of special projects and data collection. Demonstrate proficiency on the execution of key manufacturing processes which may include all or portions of the following: synthesis, cleavage and deprotection, chromatography, ultrafiltration , or freeze-drying Qualify lower levels on key manufacturing processes. May act as a lead for any given campaign. Review of basic cGMP documentation including solution and raw material reconciliation. Develop, review and revise SOPs and PIs to assure documentation reflects current operations. Qualify on basic investigational documentation including OOT, SHE, and CAPA's. Revise generic documentation to keep up with industry standards and customer expectations. Required Skills/Abilities: Minimum education requires high school diploma or equivalent with college level chemistry or equivalent work experience. A biotechnology certificate or college degree is preferred. Must have knowledge of basic laboratory instrumentation such as use of pH meter, UV instrumentation, and solution delivery systems (process skids). Must have knowledge of relevant manufacturing processes which may include chemical synthesis, chromatography, ultrafiltration, freeze-drying, and aseptic technique. Experience in cGMP manufacturing environment. The annualized salary range for this position is $74,200.00 - $90,700.00.

Work Schedule 12 hr shift/days Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Operating equipment is used to manufacture products. Weighs, measures and checks raw materials to ensure that batches manufactured contain proper ingredients in proper quantities. Fully trained and proficient at manufacturing drug product injectables in a cleanroom environment and following GMP standards. Autonomously run equipment, pumps, and automated systems and collaborate with team members to ensure it's right the first time and on schedule. Perform operations in Support Services, Upstream, Downstream, and Fill/Finish workstreams following SOPs and Batch records and recommending improvements. Work Hours: This position will generally require the ability to work a 12-hour rotating shift in a 24-hour, 7 day per week operation to include holidays. This role is a 1st shift, 7am-7pm shift (2/2/3 Rotation). Responsibilities Optimally complete work instructions while following procedures and cGMP regulations. Applications of acquired job skills and company policies and procedures to complete assigned task Fully trained on all unit operations associated with the department. Works on assignments that are semi-routine in nature but receives instruction on new processes that are accepted practices Follows established procedures on routine work, requires instructions only on new assignments. Stays up to date on required job training. Maintains inventory records of raw materials used in batch manufacturing. Keeps accurate and up-to-date batch records and data sheets on batches in process. Inspect finished product to assure adherence to specifications such as appearance, foreign substances and packaging or labeling requirements as required Assist with manufacturing batch records reconciliation. Complete assigned work tasks on time. Adhere to SOP's, Batch Records, and Wok Instructions by living the Quality values every day and holds peers across the site accountable as well. Support the on-time closure of Nonconformance's/ CAPAs. Assist in the completion and identification of PPI initiatives and continuous improvements. Identify and communicate items requiring customer concern; complete post critical issue decisions. Accurately records and analyzes batches against standards all processing data gathered from instruments, etc. to ensure operating standards are met. Make approved adjustments as appropriate to maintain process parameters within designated limits. Maintain a culture of safety by identification of near misses, safety walkthroughs and assisting with resolution of safety observations. Ensure chemicals are properly stored and labeled. 90% of time spent on the floor Education/Experience/Equivalency Requirements: High School Diploma or Equivalent Minimum of 2 years' experience in manufacturing/operations Knowledge, Skills and Abilities: Ability to perform aseptic operations. Surface level problem solving skills. Ability to anticipate system response. Understand cleanroom concepts. Ability to follow directions & procedures and work in team environment. Strong attention to detail and aim to accomplish the job timely, accurately and safely the first time is required, as well as the ability to work closely and effectively in a team environment. Ability to apply knowledge of Good Manufacturing processes and the knowledge and skills in pharmaceutical processes, equipment, instrumentation, and procedures. Adhere to all Personal Protective Equipment (PPE) requirements used within cGMP manufacturing. Physical Requirements: Employee is regularly required to stand; use hands to finger, handle, or feel; reach with hands and arms; sit and to talk or hear. The employee is required to walk and stoop or kneel/crouch up to 50% of the time. The employee is required to ascend/ descend ladders, and push, pull, or lift a maximum of 50 lbs. Employee may be asked to sit continuously for a maximum of 6 hours. Specific vision abilities required by this job include close vision and ability to adjust focus with tasks. We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our distributed team of more than 75,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit ********************* Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status. Compensation and Benefits The hourly pay range estimated for this position based in Massachusetts is $23.02-$38.36. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: *****************************************************

Precix is seeking dedicated individuals for the role of Manufacturing Associate, both entry-level and experienced, to join our team and contribute to our mission of being a manufacturing leader in sealing solutions. At Precix, we pride ourselves on our commitment to quality, innovation, and continuous improvement, allowing us to consistently exceed our customers' expectations. Our collaborative approach leverages extensive engineering expertise and a creative mindset to design solutions that perform exceptionally well, even in extreme conditions. We foster a culture rooted in integrity, transparency, and diversity, valuing the contributions of our employees and forging strong relationships with our customers and suppliers. As a Manufacturing Associate, you will play a vital role in our production process and help create the high-quality sealing solutions that our customers rely on. If you are looking to develop your skills in a dynamic environment that prioritizes teamwork and growth, we invite you to be part of the Precix team and help us make a meaningful impact in the world. Responsibilities Assist in the manufacturing process by operating machinery and equipment according to company standards. Conduct quality checks on products to ensure they meet Precix's high-quality standards. Maintain a clean and organized work environment to promote safety and efficiency. Collaborate with team members to ensure smooth workflow and meet production deadlines. Follow production schedules and adjust work as needed to achieve goals. Participate in training and development programs to enhance skills and advance career. Report any issues or discrepancies in the production process to supervisors promptly. Requirements High school diploma or equivalent; some technical training or experience in manufacturing is a plus. Ability to work effectively in a team-oriented environment. Good communication skills and the ability to understand instructions clearly. Strong attention to detail and a commitment to quality work. Willingness to learn and adapt to new processes and equipment. Basic problem-solving skills and a proactive approach to work. Ability to stand for extended periods, lift heavy objects, and perform physically demanding tasks. Benefits Health Care Plan (Medical, Dental & Vision) Life Insurance (Basic, Voluntary & AD&D) Family Leave (Maternity, Paternity) Short Term & Long Term Disability Training & Development Employee Assistance Program - Counseling Paid Time Off

Job DescriptionPosition Title: Manufacturing Associate I Reports to: Director, Manufacturing Status: Regular, Full-Time, Exempt Company Summary: Stratus Therapeutics is a stem cell therapeutic company developing an innovative platform technology for generating self-renewing blood stem cells. We have breakthrough potential to provide patients with rapid and broad access to HLA-compatible transgene-free blood stem cell therapies. Stratus Therapeutics is committed to advancing science and enhancing the health and well-being of patients. This commitment, along with an exciting team culture, drives our efforts to develop an off the shelf stem cell therapeutic platform. Position Summary: Stratus Therapeutics is seeking a motivated Manufacturing Associate/Sr. Manufacturing Associate to support routine GMP Manufacturing operations. This includes day-to-day operational tasks including but not limited to Cell Culture in a clean room environment, GMP Materials Logistics, and Environmental Monitoring within Stratus GMP manufacturing space. This is an on-site role, primarily in Watertown, MA with occasional work in Cambridge MA. Some travel between sites is required. Specific responsibilities include, but are not limited to: Perform, verify, and support GMP Cell Culture manufacturing activities in a cleanroom environment Complete applicable GMP Manufacturing Batch Records, Forms, and associated documentation Support GMP materials release and labeling Transfer materials into the GMP cleanroom suites following proper wipe down procedures. Follow Personnel, Material, and Waste flow procedures related to GMP manufacturing of Cell Therapy products Restock cleanroom manufacturing areas as needed. Perform environmental monitoring sampling when needed. Support deviation investigations and CAPA activities Other related duties as needed Qualifications include: Associates degree is required (in a science-related discipline preferred) BA/BS degree preferred 0- 2 years of professional work experience in a cell based therapeutic product is preferred Strong interpersonal skills & attention to detail Strong commitment to teamwork, collaboration, and professionalism Proficiency in working with MS Office Suite Able to handle a dynamic workload, multi-task, and perform effectively under tight deadlines Must be able to lift 30 lbs. AAP/EEO Statement Stratus Therapeutics is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. We are committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics. Powered by JazzHR LiRzMPOiRn

Neurotech Pharmaceuticals is an innovative biopharmaceutical company located in Cumberland, RI and Needham, MA, within Greater Boston's vast biotechnology landscape. Since our inception more than 20 years ago, we have been developing a proprietary drug delivery platform, Encapsulated Cell Technology (ECT), designed to deliver genetically modified therapeutics to slow the progression of chronic retinal diseases. Our most advanced program is delivering a neurotrophic factor to treat the orphan disease Macular Telangiectasia Type 2 (MacTel), a rare retinal disorder, by leveraging ECT's innovative approach providing sustained, targeted treatment directly to the eye.

Neurotech Pharmaceuticals, Inc. is a private biotech company located in Cumberland, RI and Needham, MA, within the realm of Greater Boston's vast biotechnology landscape. Since our inception more than 20 years ago, our focus has been on developing and commercializing transformative therapies for chronic eye diseases. The core platform technology, Encapsulated Cell Therapy (ECT), is a first-in-class drug delivery platform designed to slow the progression of chronic eye diseases. Neurotech's first commercial product, ENCELTO TM (revakinagene taroretcel-lwey), is approved in the United States for the treatment of adults with idiopathic Macular Telangiectasia Type 2 (MacTel). Encapsulated cell-based gene therapy is designed to provide long-term, sustained delivery of therapeutic proteins for the treatment of chronic eye diseases. We are currently seeking to add a Manufacturing Associate who will play a vital role in day-to-day, hands-on cGMP manufacturing operations. The Manufacturing Associate will be an independent thinker to monitor and troubleshoot critical processes and regularly draft and revise documents such as Batch Records and SOPs. S/he will also provide peer review of technical reports such as deviations, CAPAs and Change Controls. In addition, the Manufacturing Associate will identify, recommend and implement improvements related to routine floor operations. Job Requirements Perform basic to complex aseptic operations within an ISO 5 environment according to Batch Records and SOPs. Document all activities in Batch Records, Logbooks, Forms, etc. using Good Documentation Practices. Follow verbal and written procedures in operating production equipment and to monitor/perform process steps, while being able to identify subtle variances or escalating events that are non-routine in nature. Perform in-process testing and other tasks as assigned that ensure sustainable right-first-time performance. Lead project(s) from creation of tasks through execution and closure. Create batch records and SOPs for newly defined processes Assist with manufacturing material management. Assist with and Own quality systems. May be required to prepare, sanitize, and disinfect equipment to prevent microbial contamination Education and Experience Bachelor's degree in Science with a minimum of 2 years' experience with aseptic upstream biologic production or aseptic fill/finish processes in a GMP environment or High School Diploma/Associate's with a minimum of 4 years' experience with aseptic upstream biologic production or aseptic fill/finish processes in a GMP environment. Knowledge, Skills, and Abilities Must have cGMP manufacturing experience with the ability to interpret and apply GMP knowledge Must have Cell Culture Experience and technical understanding of adherent cell culture processes Must be detail oriented with organization and planning skills Must be proficient in Microsoft Office (Word, Outlook, Excel, Powerpoint) Ability to demonstrate technical writing capability Experience with and Basic troubleshooting skills on Manufacturing and lab equipment Support Quality and Validation activities/documentation as needed Must possess a positive attitude and willingness to perform hands-on daily operations Must be able to work independently day to day and collaboratively on project team Experience with manufacturing automated systems and electronic batch reporting a plus. Neurotech Pharmaceuticals 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.

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers . If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post. What you will do Let's do this. Let's change the world. In this vital role you will perform operations in the Manufacturing area, specifically Inoculation/Seeds. Operations will be performed according to Standard Operating Procedures (SOPs). Responsibilities include: Perform and monitor critical processes, execute routine validation protocols, Regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports. Perform basic troubleshooting and assist in the review of documentation for assigned functions. Participate on cross-functional teams and represent the Inoc/Seeds group. May also have the responsibility of owning NC/CAPA's and Change Control records. Identify, recommend, and implement improvements related to routine functions In this role, you will be expected to work a 12-hour shift (7PM-7AM) on a rotating schedule (C Shift). This includes extra benefits such as receiving an added 15% shift differential, and also getting premium pay for any Sundays worked. The schedule during the initial on-boarding phase for this role (2-6 weeks) will be administrative (Monday through Friday, approximately 8am to 5pm). What we expect of you We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a self-starter with these qualifications. Additional Qualifications/Responsibilities What you will do Let's do this. Let's change the world. In this vital role you will perform operations in the Manufacturing area, specifically Inoculation/Seeds. Operations will be performed according to Standard Operating Procedures (SOPs). Responsibilities include: Perform and monitor critical processes, execute routine validation protocols, Regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports. Perform basic troubleshooting and assist in the review of documentation for assigned functions. Participate on cross-functional teams and represent the Inoc/Seeds group. May also have the responsibility of owning NC/CAPA's and Change Control records. Identify, recommend, and implement improvements related to routine functions In this role, you will be expected to work a 12-hour shift (7PM-7AM) on a rotating schedule (C Shift). This includes extra benefits such as receiving an added 15% shift differential, and also getting premium pay for any Sundays worked. The schedule during the initial on-boarding phase for this role (2-6 weeks) will be administrative (Monday through Friday, approximately 8am to 5pm). What we expect of you We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a self-starter with these qualifications.

Cresco Labs is one of the largest public, vertically integrated, multistate operators in the cannabis industry. Our portfolio of in-house cultivated and manufactured brands features some of the highest quality, most awarded and most popular cannabis products in America. With dozens of locations nationwide, our owned and operated Sunnyside dispensaries provide a welcoming, positive, judgement-free place to shop for anyone at any point on their cannabis journey. Founded in 2013, Cresco Labs' mission is to normalize and professionalize cannabis through our passionate employees. As stewards of the cannabis industry, our teams are constantly focused on supporting the needs of our fellow colleagues, consumers, customers, and communities alike. With a focus on Social Equity and Educational Development, our SEEDTM initiative ensures that our company reflects the communities in which we serve, ensuring equal opportunity for all to have the knowledge and resources to work in and own businesses in cannabis. At Cresco Labs, we aim to revolutionize and lead the nation's cannabis industry with a focus on quality and consistency of product, and to bring legitimacy to the industry with the highest level of integrity and professionalism. If you're interested in joining our mission, click the below links to join our team today! MISSION STATEMENT At Cresco, we aim to lead the nation's cannabis industry with a focus on regulatory compliance, product consistency, and customer satisfaction. Our operations bring legitimacy to the cannabis industry by acting with the highest level of integrity, strictly adhering to regulations, and promoting the clinical efficacy of cannabis. As Cresco grows, we will operate with the same level of professionalism and precision in each new market we move in to. SCHEDULE Monday - Thursday, 6:00am - 4:30PM JOB SUMMARY Cresco Labs is seeking Lab Technician to join our facility. The Lab Technician will be responsible for assisting in product processing and formulation. The Lab Technician completes tasks assigned by the Lab Manager to monitor and maintain the organization, cleanliness and efficiency of production areas well as maintains quality control measures. The individual is also responsible for carrying out day-to-day tasks including prepping and packaging. CORE JOB DUTIES Manufacturing: Responsible for the preparation of Cresco Labs extraction, facilitating the processing of product in accordance with the commonwealth and standards set by Cresco Labs Ensures consistency and efficacy of product through quality control testing and procedures outlined by Cresco Labs Responsible for product processing and product formulation Lab bench work and product filtrations Work in various environmental conditions, including colder temperatures. Provide assistance across multiple facility departments as required. Perform data entry and documentation tasks in adherence to Good Manufacturing Practices (GMP). Lift and move objects up to 50 lbs. Facility Cleaning: Perform all assigned duties required to ensure a clean and safe production facility Ensure personal hygiene is acceptable under standards set by Cresco Labs before performing any production activities including washing hands, wearing a hair net, changing clothes, etc… Complete the sanitation of all production equipment and tools including workspace, lab equipment, containers, and appliances. REQUIRED EXPERIENCE, EDUCATION AND SKILLS Two years of experience in a laboratory or similar regulated environment with a strong focus on health and safety compliance. Past experience in a highly regulated field producing pharmaceutical or nutraceutical products preferred Effective time-management skills and ability to multi-task Flexibility to adjust work schedule based on business needs. Ability to work in a fast-paced, changing, and challenging environment Proficiency in windows-based software and point of sale applications Requires work around plant material, which could include exposure to plant pollen and/or dust. Requires ability to sit, stand, kneel, and/or do repetitive actions with your hands for long periods of time. Requires ability to lift up to 50 lbs to torso level. BENEFITS Cresco Labs is proud to offer eligible employees a robust offering of benefits including, major medical, dental and vision insurance, a 401(K)-match program, FSA/HSA programs, LTD/STD options, life insurance and AD&D. We also offer eligible employees paid holidays and paid time off. Other rewards may include annual discretionary bonuses, stock options as well as participation in our employee discount program. Benefits eligibility for permanent positions may vary by full-time or part-time roles, location, or position. In accordance with any local and state compensation laws, the compensation listed is the current estimated range for the position. Final offer details and future compensation may be determined by multiple factors including but not limited to, geographic location, market compensation data, skills, experience, and other relevant factors. For questions about this please discuss with your recruiter during the interview process. Pay Range$20-$20 USD ADDITIONAL REQUIREMENTS Must be 21 years of age or older to apply Must comply with all legal or company regulations for working in the industry Cresco Labs is an Equal Opportunity Employer and all applicants will be considered without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status. California Consumer Privacy Act ("CCPA") Notice to Applicants:Please read the California Employee Privacy Notice ("CA Privacy Notice") regarding Sunnyside* and its affiliate Cresco Labs' policies pertaining to the collection, use, and disclosure of personal information. This CA Privacy Notice supplements the information contained in the Sunnyside* Privacy Policy and applies to California resident employees and job applicants. Applicants with disabilities may access this notice in an alternative format by contacting ************************* Reporting a Scam: Cresco Labs is aware of fictitious employment offers being circulated from various sources. Many of these schemes consist of an alleged offer of employment with Cresco Labs with the intention of gaining personal information, including payment and/or banking information. Be aware that fraudulent job offers and correspondence may appear legitimate: they may feature a Cresco Labs logo, they may appear to originate from an official-looking email address or web site, or they may be sent by individuals purporting to represent Cresco Labs or an entity which includes the word Cresco Labs in its name. Please note that Cresco Labs does not ask for payment or personal banking information as a condition of employment. Any personal information is requested for payroll or state badging purposes only. Applications can be securely submitted through our career's pages.We are working diligently to block this from happening. Beware if an offer of employment looks too good to be true. Never divulge personal and banking information or send money if you are unsure of the authenticity of an email or other communication in the name of Cresco Labs.If you are in doubt, please contact us at **************************** with questions.

Join Amgen's Mission of Serving Patients At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Associate Manufacturing - Nights What you will do Let's do this. Let's change the world. In this vital role you will perform operations in the Manufacturing area, specifically Inoculation/Seeds. Operations will be performed according to Standard Operating Procedures (SOPs). Responsibilities include: * Perform and monitor critical processes, complete routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports. * Perform basic troubleshooting and assist in the review of documentation for assigned functions. * Participate on cross-functional teams and represent the Inoc/Seeds group. * May be responsible for NC/CAPA's and Change Control records. * Identify, recommend, and implement improvements related to routine functions. In this role, you will be expected to work a 12-hour shift (7PM-7AM) on a rotating schedule (D Shift). This includes extra benefits such as receiving an added 15% shift differential, and also getting premium pay for any Sundays worked. The schedule during the initial on-boarding phase for this role (2-6 weeks) will be administrative (Monday through Friday, approximately 8am to 5pm). What we expect of you We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a self-starter with these qualifications. Basic Qualifications: * High school/GED + 2 years of manufacturing or operations work experience OR * Associate's + 6 months of manufacturing or operations work experience OR * Bachelor's Preferred Qualifications: * Knowledge of small scale bioreactors, wave bioreactors, and aseptic processing. * CFR and Regulatory knowledge * Mechanical ability/expertise * Knowledge of WIP lab equipment and computers, with LIMS access * Basic statistical mathematical skills * Ability to interpret and apply GMP knowledge * Understanding of analytical methods for manufacturing area * Ability to demonstrate technical writing capability with Trackwise access * Able to demonstrate project management skills and presentation skills * Independently collaborate with outside resources * Ability to understand, apply and evaluate basic chemistry, biology and physical principles * Basic troubleshooting skills on bioreactors * Experience with Delta V, RD's * Experience with lab equipment/testing What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: * A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts * A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan * Stock-based long-term incentives * Award-winning time-off plans * Flexible work models, including remote and hybrid work arrangements, where possible Apply now and make a lasting impact with the Amgen team. careers.amgen.com In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. . Salary Range 73,359.00 USD - 85,625.00 USD

Advancing medicine to save lives. Together. Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially for patients with rare and serious diseases. Rentschler Biopharma SE is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. We offer customized full-service solutions for bioprocess development and the production of complex biopharmaceuticals. As a German family-owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best-in-class solutions - together with our clients. Rentschler Biopharma has approximately 1,400 employees and is headquartered in Laupheim, Germany, with a site in Milford, MA, USA. In 2024, we joined the United Nations Global Compact, underlining our commitment to sustainability. As an independent family-owned company, we live by the motto: Many hands, many minds - ONE TEAM! Open, respectful cooperation characterizes our working environment, where quality awareness, diligence and responsibility are our top priorities. With all the diversity of our talents in the Rentschler team, we pursue one vision together: advancing medicine to save lives. This role will follow an overnight Pitman schedule, 5pm-5am. Key Experience/ Responsibilities for Lead Upstream Manufacturing Associate Subject Matter Expert in cGMP upstream manufacturing; especially with Mammalian Cell Culture, Roller Bottles, Rocker Bioreactors, Fed batch and Profusion Bioreactors, Cell Harvest Clarification, Viral Inactivation, Buffer and Media preparation A thorough understanding of cell culture key performance indicators, cell counts, seeding densities, confluence, and the science behind the upstream production of mAb's Specific equipment/systems that we are using include Cellmate roller bottle robot, 20L/50L wave bioreactor, Cytiva 200L & 500L single use bioreactor, TCU's, BSC's, roller racks, incubators and disposable technology systems; must have a thorough understanding of the equipment and controls as this role will be the front-line troubleshooting and correction role for the shift Must have experience with initiating, developing and revising SOP's and Batch records for upstream processes Thoroughly familiar with the identification of actions and results that are outside procedures and limits which require escalation through events and deviations; responsibilities include leading and completing investigations of root causes and formally documenting/writing deviations for such events in upstream Subject matter expert for materials and the ordering of materials in time to meet the schedule; participates in inventory cycle counts and resolution/ corrective actions for discrepancies Assures that SAP transactions for process orders are executed on time and works with supply chain to resolve any discrepancies Schedules daily activities for coworkers on shift, tracks completion of activities and reports on progress to manufacturing supervisor Assures that executed batch records are reviewed thoroughly and all entries are correct before turning over to QA for approval; works to resolve batch record entry issues before they are reviewed by QA Assures activities in the suite are conducted safely and in accordance with Safety procedures Ways of Working - Leadership Capabilities Collaborates with and provides open, honest, technically accurate information to support teams (Eng, Fac, PS, QA, QC, SC) during scheduling meetings, event/deviation investigations and process/ equipment troubleshooting This position is the lead Qualified Trainer for new employees or for developing new competencies in existing/ transferred personnel; must be experienced with training models and focused on building competencies and behaviors to elevate the performance of team members Monitors team culture provides clarity to misinformation and legacy attitudes and behaviors Elevates issues early, presents issues with options for quick and compliant resolution Provides feedback and SME support for training department process improvements Provides feedback to supervisor/ manager on employees' performance on the shift Leads some team meetings and may facilitate multi-department discussions Supports a positive work environment that promotes inclusion and diversity Standard Manufacturing Duties and Responsibilities for Associates The Key Experience and Ways of working distinguish the Lead Upstream Manufacturing Associate from the Manufacturing Associate roles. However, the Lead Associate is on the floor, operating the equipment and completing batch records alongside the manufacturing associates. The following manufacturing responsibilities are also performed Perform operations of the following (may be applicable to commercial scale product, development studies, clinical scale or validation activities): Perform, Monitor, Review, and record batch parameters, including computer data entry; complete relevant paperwork following GDP/GMP guidelines; perform mathematical calculations related to production processes Pushing buffer containers ranging from 50L to 200L Sitting for periods of 2 to 3 hours Knowledge of laboratory and pharmaceutical production equipment including but not limited to autoclaves, process tanks, chromatography skids and columns, analytical equipment Lead Continuous Improvement Teams (such as 5S, Gemba, OMT, etc.) Such additional responsibilities as the Company may also assign Proficient in BSC operations and aseptic technique Qualifications With high school diploma: Normally requires 8+ years of related experience required or an associate degree in Life Sciences/Engineering field. Biotech Certificate preferred With Bachelor's degree: Normally requires 6+ years of related experience Able to read and follow detailed written instructions and have good verbal/written communication skills Able to write legibly and grammatically correct entries on records. Must be able to author technical procedures and create forms Familiar with standard troubleshooting approaches (problem statement, root cause analysis, corrections, etc.) Good computer skills, knowledge of Microsoft Word, Excel Good interpersonal skills and be able to work effectively and efficiently in a team environment Ability to work in a clean room environment and comply with hygiene standards and use of special garments; additionally, personal protective equipment must be worn due to safety requirements. Proficient in BSC operations and aseptic technique Working Conditions Normal office working conditions: computer, phone, files, fax, copier Personal Protective Equipment must be worn as required May require lifting amounts of 25 lbs Manufacturing operations tasks requires operator to regularly remain on feet for shift Physical Requirements PPE as required May require lifting amounts of 25 lbs Manufacturing operations tasks requires operator to regularly remain on feet for shift

Since its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and rare diseases. The Nobel Prize-winning CRISPR science has revolutionized biomedical research and represents a powerful, clinically validated approach with the potential to create a new class of potentially transformative medicines. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic partnerships with leading companies including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California. Position Summary Reporting to the Manufacturing Sr Manager, the Manufacturing Associate will perform manufacturing activities associated with LNP GMP manufacturing within a state-of-the-art manufacturing facility at 33 New York Ave in Framingham, MA. A successful candidate will be responsible for the manufacture of LNP therapies for clinical studies and as a commercial product. This role requires clear communication across multiple departments for the execution of daily activities. The ideal candidate will have experience successfully performing formulated LNP Manufacturing within a GMP environment. Responsibilities Perform clinical / commercial product manufacturing for LNP therapies according to cGMP standards and SOPs including Lipid and RNA Prep, T-Mix, and TFF operations Perform aseptic vial filling, visual inspection, cryopreservation, process reagent formulation, and material kitting. Transfer raw material inside cleanroom suite using sanitizing reagents or equipment. Participates in technology transfer from Process Development to the Manufacturing group. Assist in the life cycle development of Standard Operating Procedures (SOPs) for manufacturing in collaboration with PD / MSAT and Quality Systems groups. Ensures all materials and equipment are identified and available in time for manufacturing operations. Execute standard work per manufacturing schedule Participate in Quality investigations and resolutions. Ensure cGMP compliance through consistent execution. Other duties and projects as assigned to meet departmental requirements. Minimum Qualifications Certificate, associate's degree or higher in biological sciences or related fields and 2-5 years of relevant Manufacturing experience or related fields Available to work a flexible schedule as needed. Ability to don cleanroom garments and work within a classified environment (Grade B and C) Knowledge of GMP and industry standards T-Mix and TFF experience preferred Fluency in Windows and Microsoft Office applications Attentive to detail and accuracy Ability to effectively communicate and collaborate with internal stakeholders is essential Ability to work effectively in a collaborative team environment where results are achieved through influence and the incorporation of multiple points of view. Ability to execute and follow-through to completion Ability to lift 40 pounds Ability to stand for 6 hours in a clean room environment Self-driven, independently motivated, data driven and excellent problem-solving ability Competencies Collaborative - Openness, One Team Undaunted - Fearless, Can-do attitude Results Orientation - Delivering progress toward our mission. Sense of urgency in solving problems. Entrepreneurial Spirit - Proactive. Ownership mindset. Due to the nature of their work, our manufacturing and lab-based positions are located fully on-site. Manufacturing Associate: Base pay range of $40.00 per hour to $44.00 per hour + bonus, equity and benefits. The range provided is CRISPR Therapeutics' reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities. CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. To view our Privacy Statement, please click the following link: ***********************************************

Job Description Precix is seeking dedicated individuals for the role of Manufacturing Associate, both entry-level and experienced, to join our team and contribute to our mission of being a manufacturing leader in sealing solutions. At Precix, we pride ourselves on our commitment to quality, innovation, and continuous improvement, allowing us to consistently exceed our customers' expectations. Our collaborative approach leverages extensive engineering expertise and a creative mindset to design solutions that perform exceptionally well, even in extreme conditions. We foster a culture rooted in integrity, transparency, and diversity, valuing the contributions of our employees and forging strong relationships with our customers and suppliers. As a Manufacturing Associate, you will play a vital role in our production process and help create the high-quality sealing solutions that our customers rely on. If you are looking to develop your skills in a dynamic environment that prioritizes teamwork and growth, we invite you to be part of the Precix team and help us make a meaningful impact in the world. Responsibilities Assist in the manufacturing process by operating machinery and equipment according to company standards. Conduct quality checks on products to ensure they meet Precix's high-quality standards. Maintain a clean and organized work environment to promote safety and efficiency. Collaborate with team members to ensure smooth workflow and meet production deadlines. Follow production schedules and adjust work as needed to achieve goals. Participate in training and development programs to enhance skills and advance career. Report any issues or discrepancies in the production process to supervisors promptly. Requirements High school diploma or equivalent; some technical training or experience in manufacturing is a plus. Ability to work effectively in a team-oriented environment. Good communication skills and the ability to understand instructions clearly. Strong attention to detail and a commitment to quality work. Willingness to learn and adapt to new processes and equipment. Basic problem-solving skills and a proactive approach to work. Ability to stand for extended periods, lift heavy objects, and perform physically demanding tasks. Benefits Health Care Plan (Medical, Dental & Vision) Life Insurance (Basic, Voluntary & AD&D) Family Leave (Maternity, Paternity) Short Term & Long Term Disability Training & Development Employee Assistance Program - Counseling Paid Time Off

Job Description Neurotech Pharmaceuticals, Inc. is a private biotech company located in Cumberland, RI and Needham, MA, within the realm of Greater Boston's vast biotechnology landscape. Since our inception more than 20 years ago, our focus has been on developing and commercializing transformative therapies for chronic eye diseases. The core platform technology, Encapsulated Cell Therapy (ECT), is a first-in-class drug delivery platform designed to slow the progression of chronic eye diseases. Neurotech's first commercial product, ENCELTOTM (revakinagene taroretcel-lwey), is approved in the United States for the treatment of adults with idiopathic Macular Telangiectasia Type 2 (MacTel). Encapsulated cell-based gene therapy is designed to provide long-term, sustained delivery of therapeutic proteins for the treatment of chronic eye diseases. We are currently seeking to add a Manufacturing Associate who will play a vital role in day-to-day, hands-on cGMP manufacturing operations. The Manufacturing Associate will be an independent thinker to monitor and troubleshoot critical processes and regularly draft and revise documents such as Batch Records and SOPs. S/he will also provide peer review of technical reports such as deviations, CAPAs and Change Controls. In addition, the Manufacturing Associate will identify, recommend and implement improvements related to routine floor operations. Job Requirements Perform basic to complex aseptic operations within an ISO 5 environment according to Batch Records and SOPs. Document all activities in Batch Records, Logbooks, Forms, etc. using Good Documentation Practices. Follow verbal and written procedures in operating production equipment and to monitor/perform process steps, while being able to identify subtle variances or escalating events that are non-routine in nature. Perform in-process testing and other tasks as assigned that ensure sustainable right-first-time performance. Lead project(s) from creation of tasks through execution and closure. Create batch records and SOPs for newly defined processes Assist with manufacturing material management. Assist with and Own quality systems. May be required to prepare, sanitize, and disinfect equipment to prevent microbial contamination Education and Experience Bachelor's degree in Science with a minimum of 2 years' experience with aseptic upstream biologic production or aseptic fill/finish processes in a GMP environment or High School Diploma/Associate's with a minimum of 4 years' experience with aseptic upstream biologic production or aseptic fill/finish processes in a GMP environment. Knowledge, Skills, and Abilities Must have cGMP manufacturing experience with the ability to interpret and apply GMP knowledge Must have Cell Culture Experience and technical understanding of adherent cell culture processes Must be detail oriented with organization and planning skills Must be proficient in Microsoft Office (Word, Outlook, Excel, Powerpoint) Ability to demonstrate technical writing capability Experience with and Basic troubleshooting skills on Manufacturing and lab equipment Support Quality and Validation activities/documentation as needed Must possess a positive attitude and willingness to perform hands-on daily operations Must be able to work independently day to day and collaboratively on project team Experience with manufacturing automated systems and electronic batch reporting a plus. Neurotech Pharmaceuticals 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.

**Join Amgen's Mission of Serving Patients** At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do. Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. **Associate Manufacturing - Nights** **What you will do** Let's do this. Let's change the world. In this vital role you will perform operations in the Manufacturing area, specifically Inoculation/Seeds. Operations will be performed according to Standard Operating Procedures (SOPs). Responsibilities include: + Perform and monitor critical processes, complete routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports. + Perform basic troubleshooting and assist in the review of documentation for assigned functions. + Participate on cross-functional teams and represent the Inoc/Seeds group. + May be responsible for NC/CAPA's and Change Control records. + Identify, recommend, and implement improvements related to routine functions. In this role, you will be expected to work a 12-hour shift (7PM-7AM) on a rotating schedule (D Shift). This includes extra benefits such as **receiving an added 15% shift differential, and also getting premium pay for any Sundays worked.** The schedule during the initial on-boarding phase for this role (2-6 weeks) will be administrative (Monday through Friday, approximately 8am to 5pm). **What we expect of you** We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a self-starter with these qualifications. **Basic Qualifications:** + High school/GED + 2 years of manufacturing or operations work experience OR + Associate's + 6 months of manufacturing or operations work experience OR + Bachelor's **Preferred Qualifications:** + Knowledge of small scale bioreactors, wave bioreactors, and aseptic processing. + CFR and Regulatory knowledge + Mechanical ability/expertise + Knowledge of WIP lab equipment and computers, with LIMS access + Basic statistical mathematical skills + Ability to interpret and apply GMP knowledge + Understanding of analytical methods for manufacturing area + Ability to demonstrate technical writing capability with Trackwise access + Able to demonstrate project management skills and presentation skills + Independently collaborate with outside resources + Ability to understand, apply and evaluate basic chemistry, biology and physical principles + Basic troubleshooting skills on bioreactors + Experience with Delta V, RD's + Experience with lab equipment/testing **What you can expect of us** As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: + A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts + A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan + Stock-based long-term incentives + Award-winning time-off plans + Flexible work models, including remote and hybrid work arrangements, where possible **Apply now and make a lasting impact with the Amgen team.** **careers.amgen.com** In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. **Application deadline** Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.