Quality Compliance & CAPA Training Specialist

Grove Technical Resources, INC; Boston (MA); On-site; USD 70,000 - 75,000; Full time

Job summary

A leading technical resources firm is seeking a GMP CAPA & Training Specialist in Boston, MA. You will manage CAPA processes, oversee training, and ensure compliance in a biopharmaceutical environment. Candidates should have a Bachelor’s degree, 8+ years of industry experience, and proficiency in Veeva and Excel. This role is specialized for individuals with strong analytical skills and familiarity with GMP regulations.

Qualifications

• 8+ years in the biopharmaceutical industry.
• Detail-oriented with strong analytical/problem-solving skills.
• Familiarity with metrics, deviation management, and manufacturing processes.

Responsibilities

• Manage open CAPAs through closure.
• Oversee training structures and ensure compliance.
• Coordinate across functions to maintain compliance.

Skills

Cross-Functional Collaboration

Strong Communication

Education

Bachelor’s in Life Sciences/Engineering or related field

Tools

Veeva

Excel

Job description

Quality Compliance & CAPA Training Specialist

Quality Compliance & CAPA Training Specialist

2 days ago Be among the first 25 applicants

Direct message the job poster from Grove Technical Resources, INC

Senior Recruiting Manager @ Grove Technical Resources, INC | Team Leadership, Recruitment

Job Title: GMP CAPA & Training Specialist– Biopharma

Location: Boston, MA (Fully Onsite)

Duration: 12+ Months Contract

Logistics: Onsite every day. Parking is the candidate's responsibility.

Overview:

Seeking an experienced CAPA & Training Lead to manage open CAPAs through closure, oversee training structures, and ensure compliance within GMP-regulated biopharma manufacturing. Must be adept in Veeva, Excel, and compliance metrics, with a strong grasp of deviation reports, triage, and cross-functional coordination.

Key Skills:

• Cross-Functional Collaboration – manage competing priorities in a matrixed environment

• Strong Communication – written, verbal, and presentation skills.

Qualifications:

• Bachelor’s in Life Sciences/Engineering or related field

• 8+ years in the biopharmaceutical industry

• Detail-oriented with strong analytical/problem-solving skills

• Familiarity with metrics, deviation management, and manufacturing processes (cell/gene therapy a plus).

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Engineering, Product Management, and Design

• Industries

  Medical Practices, Medical Equipment Manufacturing, and Biotechnology Research

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