What are the responsibilities and job description for the QA RA Compliance Specialist position at BC Forward?
Job Title: QA RA Compliance SpecialistLocation: (St. Petersburg, FL)
Duration: Contract - 6 months with possible extension
Pay Range: $30.00/hr (W2)
Job ID: 372171
Worksite: Onsite
Schedule: Monday to Friday, 8:00 a.m. to 5:00 p.m. or 9:00 a.m. to 6:00 p.m. About BCforwardBCforward is a leading global IT consulting and workforce solutions firm providing services and support to Fortune 500 and government clients. Founded in 1998, BCforward has grown with our customers needs into a full-service business solutions provider. With delivery centers and offices across North America and India, we take pride in building long-term relationships and delivering excellence through innovation, collaboration, and integrity. Job DescriptionWe are seeking a QA RA Compliance Specialist to join our dynamic team. The ideal candidate will have strong experience in change control management, regulatory submissions, and quality systems and a proven ability to drive compliant outcomes across audits, investigations, and product quality initiatives.Responsibilities:
Email: [Recruiter Email]
Phone: [Recruiter Phone Number]
Duration: Contract - 6 months with possible extension
Pay Range: $30.00/hr (W2)
Job ID: 372171
Worksite: Onsite
Schedule: Monday to Friday, 8:00 a.m. to 5:00 p.m. or 9:00 a.m. to 6:00 p.m. About BCforwardBCforward is a leading global IT consulting and workforce solutions firm providing services and support to Fortune 500 and government clients. Founded in 1998, BCforward has grown with our customers needs into a full-service business solutions provider. With delivery centers and offices across North America and India, we take pride in building long-term relationships and delivering excellence through innovation, collaboration, and integrity. Job DescriptionWe are seeking a QA RA Compliance Specialist to join our dynamic team. The ideal candidate will have strong experience in change control management, regulatory submissions, and quality systems and a proven ability to drive compliant outcomes across audits, investigations, and product quality initiatives.Responsibilities:
- Coordinate, track, and trend facility change controls, ensuring initiation requirements are met and completed actions are verified.
- Provide initial regulatory impact assessments for change controls as required.
- Liaise with customers to ensure requirements are understood and satisfied.
- Prepare and submit A/NDA submissions (initial, amendments, supplements, annual reports, 15-day alert reports), drug master files, plant/site master files, licenses, permits, and registrations to meet FDA and State requirements, including Florida.
- Prepare and submit all federal, state, and local permits in a timely manner.
- Gather information from customers to support registration activities.
- Assist with drafting, reviewing, and approving SOPs related to regulatory functions under the direction of the Group Leader.
- Support regulatory and health authority audits by collecting requested information.
- Collaborate with SMEs and site leadership to resolve product quality issues, including investigations, CAPA initiation, and follow-up to resolution.
- Prepare Annual Product Reviews (APRs) per site procedures and timelines.
- Prepare complaint investigation reports, validate investigation scope and root cause analysis, assess batch impact, recommend corrective actions, and ensure on-time closure.
- Author additional quality system documents as assigned by QA management.
- Support cGMP compliance activities, mentor team members, participate in Internal Assessments, and facilitate compliance and CAPA Review Board meetings with follow-up actions and training.
- Assist with departmental objectives and special projects as directed by the Group Leader.
- Bachelor's degree in a scientific discipline such as Chemistry, Microbiology, or Biology.
- Minimum 3 years of experience in pharmaceutical manufacturing.
- Proven experience with change controls and change control processes.
- Demonstrated investigation writing, root cause analysis, and report writing skills; APR experience preferred.
- Regulatory affairs, quality control, or quality assurance experience.
- Working knowledge of U.S. application regulations, cGMPs, and FDA guidance.
- Strong organization skills and attention to detail.
- Effective oral and written communication skills and teamwork ability.
- Ability to manage multiple priorities and apply diplomatic problem solving.
- Proficiency with Microsoft Office (Word, Excel, PowerPoint, Access).
- Knowledge of OSHA requirements and cGMP regulations.
- PathWise certification.
- Experience preparing Annual Product Reviews.
- Competitive compensation and benefits
- Opportunities for growth with global clients
- A supportive, inclusive culture that values innovation and people
- Exposure to cutting-edge technologies and projects
Email: [Recruiter Email]
Phone: [Recruiter Phone Number]
Salary : $29 - $30