As an Actalent Quality Document Control Specialist job, you could play a key feature in maintaining and handling documentation to ensure compliance with GxP requirements. Your paintings will contain organizing, processing, and archiving crucial files, supporting the control of GxP schooling, and contributing to duties associated with regulatory documentation.
Job Title: Quality Document Control Specialist
Company: Actalent
Degree: Bachelor’s Degree preferred (or equivalent experience)
Location: Hybrid in Cambridge, MA (On-site 1-2 days per week)
Experience: 0-2 years in document control, quality assurance, or related fields
Employment Type: Full-time (40 hours per week)
Salary: $25.00 – $28.00 per hour
Actalent is seeking out a delivered-on and element-oriented Quality Document Control Specialist to enroll in our group. This complete-time, hybrid characteristic gives a thrilling possibility to artwork GxP documentation in pretty collaborative and revolutionary surroundings you are eager to gather your profession in awesome manipulation and characteristic a passion for enterprise and compliance, this function is exquisite for you.
Key Responsibilities
- GxP Documentation and Archival:
- Manage Veeva GxP documentation systems, making sure accurate documentation and archiving techniques.
- Actalent Quality Document Control Specialist job Process, type, and prepare on-net website and virtual GxP documents to keep compliance with regulatory requirements.
- Project Support:
- Assist with obligations concerning GxP documentation to decorate operational efficiency and keep awesome necessities.
- Training Administration:
- Provide manual in administering GxP schooling, making sure all institution humans are knowledgeable and compliant with applicable hints.
- Collaboration:
- Actalent Quality Document Control Specialist job Work cautiously with bypass-useful agencies to make certain seamless documentation techniques.
Qualifications
To advantage achievement in this position, candidates want to fulfill the following necessities:
- Experience: 0 – 2 years of experience in record management, pleasant assurance, or a related problem.
- Technical Knowledge: Familiarity with Veeva GxP structures and regulatory documentation strategies is incredibly right.
- Skills:
- Actalent Quality Document Control Specialist job Strong organizational and multitasking talents.
- An excellent hobby to detail and a proactive approach to trouble-fixing.
- Basic know-how of GxP thoughts and compliance requirements.
- Education: A bachelor’s diploma in an applicable location is desired however not required.
Compensation and Benefits
- Pay: Competitive hourly rate starting from $25.00 to $28.00 consistent with the ur, relying on enjoyment.
- Benefits:
- 401(ok) retirement plan with matching contributions.
- Comprehensive medical medical insurance, together with dental and imaginative and prescient insurance.
- Actalent Quality Document Control Specialist job Paid break day to help paintings-life stability.
Why Join Actalent?
Actalent is devoted to fostering professional growth and presenting a supportive surrounding for its team individuals. By joining Actalent, you’ll be a part of a business business agency enterprise enterprise that values:
- Innovation and Excellence: We constantly strive for the very first-rate requirements in super and compliance.
- Team Collaboration: Actalent Quality Document Control Specialist job A supportive way of life that emphasizes teamwork and shared success.
- Career Development: Opportunities to boost your abilities and decorate for your profession.
About the Role
This is a remarkable possibility for a person beginning their profession or looking to grow in the exceptional management and regulatory documentation area. The hybrid model allows for stability among collaborative on-net internet web page artwork and the power of far-off responsibilities. If you are enthusiastic about industrial enterprise commercial enterprise agency, compliance, and ensuring outstanding vital documentation, we inspire you to use it!
Actalent is an Equal Opportunity Employer. We have a superb time range and are committed to growing inclusive surroundings for all personnel. Apply in recent times to take the subsequent step for your quality manipulation profession!
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