Stability Programs jobs

Principal Product Quality Leader

Amgen · Posted Nov 9, 2026

Open

Remote, United States
Remote
Full-time
2+ years

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Principal Product Quality Leader

Amgen · Posted Nov 9, 2026

Open

Remote, United States
Remote
Full-time
2+ years

Apply with Referso

Scientist II, Pharmaceutical Development

Neurocrine Biosciences · Posted Nov 6, 2026

Open

San Diego, California, United States
Full-time · Mid
$111K–$151K per year
2+ years

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Represent Product Development on CMC project teams across all stages of development from early discovery through commercial launch. Provide formulation and analytical expertise to support multiple preclinical and clinical programs.

Compensation

The annual base salary we reasonably expect to pay is $110,800.00-$151,000.00... In addition, this position offers an annual bonus with a target of 20% of the earned base salary and eligibility to participate in our equity based long term incentive program.

Responsibilities

Collaborate cross-functionally with Research/Discovery, Chemical Development, Analytical Development, Clinical, Quality, Regulatory, Supply Chain, and external CDMO partners
Apply first principles of formulation and process science to design and execute preformulation and formulation development studies
Plan and execute studies using Quality by Design (QbD) principles, including Design of Experiments (DOE)
Prepare, evaluate, and optimize formulations for preclinical and clinical use
Lead pilot-scale and commercial process scale-up activities

Requirements

degree in Chemistry
Biochemistry
Chemical Engineering
Nice to have: postdoc experience

Skills

cGMP pharmaceutical manufacturing processes Quality by Design (QbD)

Senior Manager, Quality Systems

Catalent Pharma Solutions · Posted Nov 6, 2026

Open

Greendale, Indiana, United States
On-site
Full-time · Manager
7+ years

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Lead the Quality and Compliance functions at the Catalent Greendale site, overseeing a team of Quality Assurance Supervisors and Specialists for operational quality, product sampling, testing, and release.

Responsibilities

Oversee Quality and Compliance functions related to dietary supplement manufacturing
Lead a team of Quality Assurance Supervisors and Specialists responsible for operational quality, product sampling, testing, and product release
Review and approve manufacturing and packaging change controls, product formulations, label changes, deviations, corrective and preventive action plans, and customer complaints
Ensure compliance with FDA, NSF, and SQF requirements for product manufacturing and participate in internal and external audits
Develop and maintain quality and compliance policies, procedures, and guidelines

Requirements

Bachelor’s degree in science or related field (Chemistry, Microbiology, or Biology)
Nice to have: invest writing
Nice to have: root cause analysis
Nice to have: 21 CFR 111
Nice to have: 21 CFR 117

Skills

current Good Manufacturing Practice (GMP)pharmaceutical quality experience

Senior Manager, Quality Systems

Catalent · Posted Nov 6, 2026

Open

Greendale, Indiana, United States
On-site
Full-time · Manager
7+ years

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Lead the Quality and Compliance functions at the Catalent Greendale site, overseeing a team of Quality Assurance Supervisors and Specialists and ensuring compliance with industry standards and regulations.

Responsibilities

Oversee Quality and Compliance functions related to dietary supplement manufacturing
Lead a team of Quality Assurance Supervisors and Specialists
Review and approve manufacturing and packaging change controls, product formulations, label changes, deviations, corrective and preventive action plans, and customer complaints
Ensure compliance with FDA, NSF, and SQF requirements and participate in internal and external audits
Develop and maintain quality and compliance policies, procedures, and guidelines

Requirements

Bachelor’s degree in science or related field (Chemistry, Microbiology, or Biology)
Nice to have: Investigation writing
Nice to have: Regulations 21 CFR 111, 21 CFR 117, 21 CFR 211
Nice to have: GFSI
Nice to have: HACCP

Skills

Good Manufacturing Practice compliance Quality Assurance Root cause analysis Regulatory compliance (FDA, NSF, SQF)

Third Party Manufacturer and Technical Transfer QA Manager

Abbott · Posted Nov 4, 2026

Open

Istanbul, Istanbul, Turkey
N/A
10+ years

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Lead quality oversight and performance management of third‑party manufacturers across EMEA, ensuring compliance with cGMP, regulatory, and Abbott quality standards.

Responsibilities

Accountable for quality oversight and performance management of TPMs across EMEA
Monitor and evaluate TPM quality performance through metrics, site oversight, and risk‑based assessments
Serve as primary quality contact for TPMs, global QA functions, and internal stakeholders
Lead preparation, approval, implementation, maintenance, and renewal of Quality Technical Agreements
Maintain regional Approved Supplier List

Skills

Quality Assurance Quality Control cGMP sterile manufacturing non‑sterile manufacturing regulatory compliance risk‑based assessments investigations

Principal Product Quality Leader

Principal Product Quality Leader

Compensation

Responsibilities

Requirements

Skills

Benefits

Scientist II, Pharmaceutical Development

Compensation

Responsibilities

Requirements

Skills

Senior Manager, Quality Systems

Responsibilities

Requirements

Skills

Senior Manager, Quality Systems

Responsibilities

Requirements

Skills

Third Party Manufacturer and Technical Transfer QA Manager

Responsibilities

Skills

Benefits

Benefits

Benefits