Principal - QA API External Manufacturing Peptides
$65.25k - $169.4kEli Lilly
Job Summary This role provides essential Quality Assurance oversight for API External Manufacturing operations, ensuring compliance with cGMP and regulatory requirements for all products manufactured by third-party partners. Job Responsibilities Lead and manage quality aspects of external API manufacturing sites, including but not limited to batch record review, disposition, deviation management, and change control. Conduct and/or participate in quality audits of external manufacturing sites to assess compliance with cGMP, regulatory expectations, and Eli Lilly's quality standards. Review and approve quality-related documents, such as manufacturing master batch records, validation protocols and reports, stability data, and analytical methods. Collaborate cross-functionally with internal teams (e.g., Supply Chain, Regulatory Affairs, Technical Services) and external manufacturing partners to resolve quality issues and drive continuous improvement. Provide expert QA guidance and support during new product introductions and technology transfers to external manufacturers. Develop, implement, and maintain quality agreements with external manufacturing organizations. Investigate and troubleshoot complex quality incidents, deviations, and out-of-specification results, determining root causes and implementing effective corrective and preventive actions (CAPAs). Represent Eli Lilly's quality interests during regulatory inspections at external manufacturing sites. Mentor and provide technical guidance to junior QA associates. Basic Requirements Bachelor's degree in Chemistry, Biochemistry, Pharmacy, Chemical Engineering or related scientific discipline. Minimum 5 years experience in Quality Assurance within the pharmaceutical or biopharmaceutical industry, with a strong focus on API manufacturing and external supply. Experience in cGMP regulations (FDA, EMA, HPRA, etc.) and global pharmacopeial requirements. Experience in auditing external manufacturing sites. Experience in quality management systems (e.g., Veeva). Willingness to travel domestically and internationally to external manufacturing sites as required. Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1. Additional Preferences Strong understanding of API manufacturing processes, analytical techniques, and quality control principles. Demonstrated ability to make sound quality decisions and effectively communicate complex technical and quality information to diverse audiences. Excellent problem-solving, analytical, and critical thinking skills. Ability to work independently and as part of a team in a fast-paced, dynamic environment. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $65,250 - $169,400 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #J-18808-Ljbffr Eli Lilly
- ...global contract development and manufacturing organization (CDMO) that... ...controlled substances, liquid-phase peptide synthesis, solid-state... ...characterization, and highly potent APIs. Your Work Matters. At... ...notebook while practicing GDP. External Influence: Ability to lead local...PrincipalContract workLocal area
- ...-client GMP environment. You'll oversee manufacturing quality, batch disposition, and quality... ...strategic and operational oversight of QA activities across Manufacturing, Warehouse... ...offer sponsorship for work authorization. External applicants must be eligible to work in...SuggestedContract work
$113k - $156k
...stability test data. Provides QA oversight of analytical and... ...and laboratory deviations. The Principal QA Specialist provides... ...service to both internal and external customers by ensuring patient... ...with clients, laboratories, manufacturing, QA batch disposition and other...PrincipalImmediate start- ...SME for the Quality team, reporting cross-QA metrics and status for KBI and clients.... ...engages with all functions supporting the external network, including functions across our company... ..., policies, and guidelines governing the manufacture and holding of materials for our company....PrincipalFlexible hours
$173.2k - $272.6k
...sterile, non-sterile, biologic, and vaccine manufacturing, as well as associated laboratories.... ...divisional projects across internal and external sites. Identify regulatory requirements,... ...Microbiology Pharmaceutical Quality Control (QC) QA Metrics Quality Management Systems (QMS)...SuggestedRelocationVisa sponsorshipFlexible hoursShift work- Principal Quality Compliance Specialist Deviations and Client SupportSkip... ...and CAPAs in support of GMP manufacturing operations and other... ...and closure. Mentors junior QA staff in deviation/CAPA review... ...Client of deviations. Supports external client review and resolution...PrincipalImmediate start
$173.2k - $272.6k
...sterile, non-sterile, biologic, and vaccine manufacturing, as well as associated laboratories.... ...divisional projects across internal and external sites. Identify regulatory requirements... ..., Pharmaceutical Quality Control (QC), QA Metrics, Quality Management Systems (QMS...Local areaRelocationVisa sponsorshipFlexible hoursShift work- ...Role: Agentforce QA Engineer (Salesforce AI & Automation Testing) Skills: MUST HAVE 5-8 years (QA/testing with Salesforce, AI, or... ...tracking tools (e.g., Jira, Azure DevOps). • Understanding of REST API testing for agent integrations. Soft Skills • Strong...
$160k - $240k
...Solutions Group Direct Hire Fulltime position for a Workday Financials Principal Tax Technologist on a remote basis ***Important: This role is... ...Avalara solutions into ERP environments. Familiarity with XML, APIs, and cloud SaaS platforms. Bachelor's degree in Accounting,...PrincipalFull timeRemote work- ...experienced Insurance Quality Analyst. The ideal candidate will have 6+ years in the Life/Annuity domain and a strong understanding of API testing. Responsibilities include ensuring the quality of insurance products, testing both front-end functionalities and backend APIs...3 days per week
- ...automation frameworks and ensure system quality in a collaborative environment. The ideal candidate has over 5 years of experience in API testing and Java development, along with strong knowledge of AWS Cloud services and SQL. This role offers the opportunity to improve...
- ...Responsible for providing Quality Assurance support to Manufacturing Process Operations. Performs document review and approval of Master Batch... ...- Bachelor's degree - 8+ years of experience in a QA cGMP environment - QMS experience Benefit packages for...Principal
- ...Test Automation Engineer (API) Location: Remote/ Hybrid (Durham, NC / Merrimack, NH / Boston / Smithfield, RI) Duration: Long term contract Must have: API Testing preferably Cucumber based testing frameworks Writing Database SQL’s -FitNesse - with 5 or...Long term contractRemote work
- ...Analyst. This role involves ensuring the accuracy and quality of insurance products through comprehensive testing, particularly with APIs. The ideal candidate has a solid background in the Life/Annuity domain and will collaborate with teams to meet both functional and...Full time3 days per week
$118k - $162.8k
...Validation & Compliance infrastructure in a Contract Development and Manufacturing Organization (CDMO) setting. Individual will be responsible... ...a regular site presence. Minimum Requirements: ~(Principal - BS/MS and 15+ years/ Senior - BS/MS and 8+ years) experience...PrincipalContract workImmediate start- ...BioSciences, Inc in Durham, NC is seeking a Quality Specialist III to provide dedicated quality assurance support for Chemistry, Manufacturing, and Controls operations. This role includes reviewing batch releases, performing deviation assessments, and ensuring compliance...
- Insight Global is hiring a Principal Automation Engineer in Durham, North Carolina. The role involves providing technical support for ongoing operations and serving as a system owner for facilities automation systems, ensuring compliance with engineering and quality standards...Principal
- ...operate three pharmaceutical manufacturing facilities that are responsible... ...business (LoB)), Quality Assurance (QA) presence & process... ...team as needed during internal, external audits and inspections Responsible... ...and /or quality related, or API experience required, preferably...Local areaShift workDay shift
- ...This is a night shift opportunity that follows a 2-2-3 schedule. It will be eligible for a shift differential.Job SummaryThe QA Manufacturing Specialist is responsible for ensuring raw materials, products, processes, facilities, documentation, and systems conform to quality...Work at officeImmediate startShift workNight shift
- ...platform includes Pro10, an industry-leading proprietary cell line manufacturing process, and an extensive array of capsids and promoters.... ..., and technical guidance documents, both internal and external Participates in continuous improvement projects in the AD...Work experience placementLocal area
- ...platform includes Pro10™, an industry-leading proprietary cell line manufacturing process, and an extensive array of capsids and promoters.... ..., and technical guidance documents, both internal and external. Participates in continuous improvement projects in the...Local area
- Powersecure-Inc. in Durham, NC is seeking a Switchgear Quality Control Technician to ensure that manufactured switchgear meets necessary electrical codes and functions as designed. The ideal candidate will have a high school diploma, experience in electrical systems, and...
- ...breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and... ...Experience in QC analysis of proteins, antibodies, peptides, or vaccines a plus, but not required Excellent verbal and...Full timeContract workImmediate start
- ...0 countries and regions. Summary: Ensures current Good Manufacturing Practices (cGMP) and FDA/Grifols Quality Systems through the... ...distribute monthly reports · Generate compliance metrics based on external inspection and internal audit data · Work with other...Full timeWork at office
- KBI Biopharma is looking for a QA Manufacturing Specialist responsible for ensuring product quality and compliance with regulations and internal procedures. This position provides oversight for bulk drug substance manufacturing activities and requires experience in a GMP...Night shift
$20 - $22.88 per hour
Corning Inc. seeks a Manufacturing Associate for the 12hr Day Shift in Durham, NC. This position requires a High School Diploma or GED and 6-12 months experience in a manufacturing environment. Responsibilities include operating production equipment, maintaining safety...Hourly payDay shift$18 - $22 per hour
Freudenberg Group is seeking a Process Technician in Durham, North Carolina. This role involves supporting manufacturing processes and ensuring quality standards in a diverse environment. Candidates should have a high school diploma and experience in manufacturing, along...Hourly pay- Initial Therapeutics, Inc. is seeking a Lead QA Floor Lead Tech to ensure safe drug product quality in Durham, North Carolina. This role involves supporting GMP operations, monitoring quality systems, and overseeing documentation compliance. The ideal candidate will have...
$87.86k - $168.9k
...adherence to policy and procedure, compliance with internal and external regulatory bodies, pharmacy sales, expense control and... ...customers inclusive of patients, prescribers, pharmaceutical manufacturers, payers, and health systems. Reports prescription errors immediately...Full timeLocal areaImmediate start$160.4k - $237.32k
...Silicon validation and debug. Experience with Gate Level Simulations. Excellent communication skills to interface internally and externally with all levels of the organization and to participate in problem-solving and quality improvement activities. Demonstrates...PrincipalPermanent employmentInternshipWork from homeFlexible hoursNight shift
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