QA Operations Specialist - Biopharmaceutical Manufacturing
SOKOL GxP Services, Oklahoma City, OK, United States
QA Operations Specialist
We are seeking a QA Operations Specialist to support Quality Assurance activities within a biopharmaceutical manufacturing environment at the LSCC site in Devens, MA. This role provides on-the-floor QA support to manufacturing operations, ensuring compliance with company policies, procedures, and global cGMP requirements.
The QA Operations Specialist performs real-time batch record review, reviews manufacturing shop floor documentation, and supports quality decision‑making in a regulated GMP environment. The role requires independent judgment, strong documentation skills, and the ability to partner effectively with manufacturing and cross‑functional teams.
This is an intermediate‑level role requiring 4–7 years of relevant experience.
Work Schedule
This position follows a rotating two‑week schedule with 12.5‑hour shifts (5:00 AM – 5:30 PM).
Week 1
Work: Tuesday, Wednesday
Off: Thursday, Friday>Work: Saturday, Sunday, Monday
Week 2
Off: Tuesday, Wednesday
Work: Thursday, Friday
Off: Saturday, Sunday, Monday
The two‑week rotation repeats continuously. Holidays are worked as business needs require.
Key Responsibilities
Provide on‑the‑floor QA support to manufacturing operations;
Ensure compliance with approved procedures and batch records;
Perform real‑time review of manufacturing batch records;
Review and approve shop‑floor manufacturing documentation;
Identify, assess, and elevate quality issues as appropriate;
Support deviation investigations, change controls, and CAPA activities;
Apply Quality Risk Management principles in daily decision‑making;
Partner cross‑functionally to support continuous improvement initiatives;
Develop and revise GMP procedures as required.
Must Haves
Required manufacturing shop floor documentation experience.
Strong authorship skills with the ability to critically review investigations, interpret results, and generate technical conclusions consistent with Quality Risk Management principles.
Required Qualifications
Associate’s or Bachelor’s degree in a relevant discipline.
Minimum 4 years of relevant Quality Assurance experience in an FDA‑regulated cGMP environment.
Strong knowledge of US and global cGMP requirements.
Experience supporting GMP manufacturing and/or warehousing operations.
Working knowledge of quality processes including deviations, investigations, change control, material disposition, product complaints, and CAPA management.
Ability moderate direction on complex tasks.
Confidence in making decisions for non‑routine quality issues.
Strong written and verbal communication skills.
Strong organizational skills with the ability to multitask in a fast‑paced manufacturing environment.
Compensation and Benefits
Competitive hourly rate: $50 – $57.8/hr (W-2 only, no C2C)
12‑month contract with possible extension
Health insurance, holiday pay, 401(k) program, and other benefits
Employee referral bonus program
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We are seeking a QA Operations Specialist to support Quality Assurance activities within a biopharmaceutical manufacturing environment at the LSCC site in Devens, MA. This role provides on-the-floor QA support to manufacturing operations, ensuring compliance with company policies, procedures, and global cGMP requirements.
The QA Operations Specialist performs real-time batch record review, reviews manufacturing shop floor documentation, and supports quality decision‑making in a regulated GMP environment. The role requires independent judgment, strong documentation skills, and the ability to partner effectively with manufacturing and cross‑functional teams.
This is an intermediate‑level role requiring 4–7 years of relevant experience.
Work Schedule
This position follows a rotating two‑week schedule with 12.5‑hour shifts (5:00 AM – 5:30 PM).
Week 1
Work: Tuesday, Wednesday
Off: Thursday, Friday>Work: Saturday, Sunday, Monday
Week 2
Off: Tuesday, Wednesday
Work: Thursday, Friday
Off: Saturday, Sunday, Monday
The two‑week rotation repeats continuously. Holidays are worked as business needs require.
Key Responsibilities
Provide on‑the‑floor QA support to manufacturing operations;
Ensure compliance with approved procedures and batch records;
Perform real‑time review of manufacturing batch records;
Review and approve shop‑floor manufacturing documentation;
Identify, assess, and elevate quality issues as appropriate;
Support deviation investigations, change controls, and CAPA activities;
Apply Quality Risk Management principles in daily decision‑making;
Partner cross‑functionally to support continuous improvement initiatives;
Develop and revise GMP procedures as required.
Must Haves
Required manufacturing shop floor documentation experience.
Strong authorship skills with the ability to critically review investigations, interpret results, and generate technical conclusions consistent with Quality Risk Management principles.
Required Qualifications
Associate’s or Bachelor’s degree in a relevant discipline.
Minimum 4 years of relevant Quality Assurance experience in an FDA‑regulated cGMP environment.
Strong knowledge of US and global cGMP requirements.
Experience supporting GMP manufacturing and/or warehousing operations.
Working knowledge of quality processes including deviations, investigations, change control, material disposition, product complaints, and CAPA management.
Ability moderate direction on complex tasks.
Confidence in making decisions for non‑routine quality issues.
Strong written and verbal communication skills.
Strong organizational skills with the ability to multitask in a fast‑paced manufacturing environment.
Compensation and Benefits
Competitive hourly rate: $50 – $57.8/hr (W-2 only, no C2C)
12‑month contract with possible extension
Health insurance, holiday pay, 401(k) program, and other benefits
Employee referral bonus program
#J-18808-Ljbffr