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Tpm Qa Manager Jobs (NOW HIRING)

Who We Are TPM Laboratories, Inc. is an independent contract testing laboratory providing ... Scope of the Role The QA Manager leads TPM Laboratories' quality system and ensures laboratory work ...

The QA Manager will be part of Operations, reporting directly to the Business Unit Leader; any conflicts between Operations and Quality will be addressed through the Group Business Unit Leader. * All ...

... pursuit of TPM, serve as primary lead for Q pillar * Develop initiatives to improve plant ... QA experience with 5 or more years of QA management experience within consumer products ...

Quality Assurance Manager

Kingfield, ME · On-site

$101K - $128K/yr

... pursuit of TPM, serve as primary lead for Q pillar * Develop initiatives to improve plant ... QA experience with 5 or more years of QA management experience within consumer products ...

Quality Assurance Manager

Kingfield, ME · On-site

$101K - $128K/yr

... pursuit of TPM, serve as primary lead for Q pillar * Develop initiatives to improve plant ... QA experience with 5 or more years of QA management experience within consumer products ...

Quality Assurance Manager

Kingfield, ME · On-site

$101K - $128K/yr

... pursuit of TPM, serve as primary lead for Q pillar * Develop initiatives to improve plant ... QA experience with 5 or more years of QA management experience within consumer products ...

Quality Assurance Manager - Indiana Our food production client, located in the central part of Indiana, is actively seeking a Quality Assurance Manager. The QA Manager directly leads the QA ...

The Role The QA Manager will embody WiCell's culture of quality and values and align daily actions with departmental goals. The QA Manager requires the ability to evaluate, investigate, solve ...

Quality Assurance Manager

Aiken, SC · On-site

$100 - $125/hr

Quality Assurance Manager As a Quality Assurance Manager at C.A. Murren and Sons, you will be considered an important part of the team as you bring your expertise in meeting organizational objectives.

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Tpm Qa Manager information

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How much do tpm qa manager jobs pay per year?

As of Sep 9, 2026, the average yearly pay for tpm qa manager in the United States is $118,074.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $144,500.00 per year, depending on experience, location, and employer.

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Infographic showing various Tpm Qa Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $118,074 per year, or $56.8 per hour.

Quality Assurance Manager

Cherry Hill, NJ • On-site

Focus Lab
11 - 50 employees

$125 - $150/hr

Other

Posted 21 days ago


Job description

Who We Are

TPM Laboratories, Inc. is an independent contract testing laboratory providing personalized analytical services to the pharmaceutical and chemical industries. TPM Labs specializes in Analytical Research and Development Testing Services, Quality Control Testing and Stability Storage & Testing Services.

Our goal is to provide high quality, cost effective and timely service, personalized to meet your needs.

Scope of the Role

The QA Manager leads TPM Laboratories’ quality system and ensures laboratory work meets cGMP, FDA, ICH, USP, and internal requirements. This role exists to protect data integrity, keep the site inspection-ready, and provide clear QA governance across documentation, investigations, and releases.

Key responsibilities include leading QA staff; maintaining QA policies, SOPs, and controlled documents; approving methods, specifications, and validation protocols; reviewing analytical data for accuracy and compliance; overseeing OOS/OOT, deviations, CAPA, and change control; trending quality events; managing internal audits; supporting client and regulatory audits; and driving GMP training and continuous improvement.

Required qualifications/skills:

  • Bachelor’s in Chemistry (or related discipline)
  • 6–8 years in a regulated pharmaceutical/laboratory environment
  • Strong QA systems, audit, and compliance oversight experience
  • Proven review/approval of scientific and regulatory documentation
  • People leadership experience; strong knowledge of ALCOA+ and 21 CFR 210/211
Your Typical Day

You start by checking the status of open quality events and the lab’s inspection-readiness items, then confirm priorities with senior leadership. Mid-morning is focused time for document review—data packages, controlled records, and technical reports—so releases and client timelines stay on track.

As the day moves on, you shift between short, agenda-led team touchpoints and deeper problem-solving sessions where you align QA expectations with operational realities. You may host or prepare for a client audit, review responses and commitments, or brief teams on a regulatory update.

Before the day ends, you look ahead: confirm resources and schedules, ensure projects are logged correctly in Pryme, and identify one practical improvement to strengthen compliance without slowing delivery.

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