Deviation Investigator Job at Brooksource, Concord, NC

MVZTS29PV21wZXloQ090elpFQnRSTmNC
  • Brooksource
  • Concord, NC

Job Description

Deviation Investigation Support – Operations

Location: On-site in Concord, NC

Engagement Type: 6–12 month contract (with potential for extension)

Company: Brooksource Engineering Services

Client: Pharmaceutical Manufacturing Partner

Position Overview

Brooksource Engineering Services is seeking a Deviation Investigator to support our pharmaceutical manufacturing client in Concord, NC. This is a contract role (6–12 months) with the potential for extension, ideal for professionals with 3–5 years of experience in technical writing, root cause analysis, and quality engineering.

This role focuses on writing deviations for a production line that is not yet commercially approved. The position begins with extensive training and study of existing lines, with deviations expected to gradually increase. This is a capacity-driven role and a great opportunity to contribute to a growing operation.

Key Responsibilities

  • Conduct thorough investigations into deviations, identifying root causes and contributing factors using engineering-based RCA methodologies.
  • Write clear, concise, and technically sound deviation reports.
  • Collaborate with cross-functional teams to gather information and ensure timely resolution of deviations.
  • Apply critical thinking and technical knowledge to recommend effective corrective and preventive actions (CAPAs).
  • Ensure compliance with internal procedures and regulatory standards.

Requirements

  • 3–5 years of experience in a technical or quality-focused role.
  • Strong technical writing skills, with the ability to clearly explain complex issues.
  • Experience with root cause analysis (RCA), preferably in an engineering discipline.
  • Proficiency in Microsoft Office Suite or similar tools.
  • Excellent communication and analytical skills.
  • Ability to work independently and manage shifting priorities.

Preferred Qualifications

  • Background in engineering, life sciences, or quality engineering (preferred over quality assurance).
  • Experience in pharmaceutical or biotech manufacturing environments.
  • Familiarity with deviation management systems and CAPA processes.

Additional Information

  • Shift: Regular business hours (8:00 AM – 5:00 PM).
  • Training: Extensive onboarding and training provided.
  • Workload: Initial phase will be training-heavy with deviations expected to increase over time.
  • Candidates without direct pharma or manufacturing experience are encouraged to apply if they meet the core requirements.

Job Tags

Contract work, Shift work,

Similar Jobs

Lutz

Data Analyst Job at Lutz

 ...and work-life balance is more than just a buzzword. TECH | DATA ANALYTICS Lutzs Data Analytics team bridges the gap between...  ...here, and we think you will, too. MAKE AN IMPACT As a Data Analyst, you will : Understand client needs and translate them into... 

Russell Tobin

Assistant General Manager Job at Russell Tobin

Title: Assistant General Manager Location: East Village, NY Salary: $85,000 We are seeking an experienced and passionate Assistant General Manager (AGM) to join our dynamic team! The AGM is responsible for overseeing daily restaurant operations, ensuring high...

IMCS Group

Injection Molding Operator Job at IMCS Group

 ...quality development and confirmation of new model plastic shop mold and equipment processes to ensure KPIs are achieved prior to the...  ...Centers. Providing hands-on support of new model injection molding preparation and trials Identifying mold and or equipment... 

The Method Staffing

Bookkeeper Job at The Method Staffing

 ...estate sector, located in Boca Raton, FL. With continued business expansion, they are seeking a detail-oriented and experienced Bookkeeper to support day-to-day accounting operations. This is a great opportunity to join a stable, growth-oriented team. The client is... 

The Packaging Company

Quality Manager (U.S.-Based, International Oversight) Job at The Packaging Company

 ...testing, and validations to ensure compliance with specifications. Communicate regularly with teams across time zones; may require early morning or evening meetings. Ensure compliance with applicable ISO standards and regulatory requirements (e.g., ISO 9001, FDA, RoHS,...