Document Control Specialist I
- The Quality Document Technician is responsible for various assignments supporting Company quality systems and ensuring that required documents are created and organized for use in manufacturing and for releasing products.
job type: Contract
salary: $18.00 - 21.63 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
- Makes detailed observations, analyzes data, and interprets results.
- Create, verify, and distribute quality documentation required for manufacturing.
- Support Document Center Technicians with standard office work and for batch release.
- Maintains department equipment and inventory levels for controlled materials.
- Identifies process improvements and escalates to Quality Supervision and/or Management.
- Ability to work independently and as part of a team in a fast-paced environment.
qualifications:
- 6 months of experience in manufacturing/quality preferred
- HS Diploma or equivalent is required
- Basic science, math, and digital literacy (including Microsoft Word and Excel) are required.
- Strong writing and verbal communication abilities, as well as problem solving capabilities are needed.
- Attention to detail and organization are highly desired
- It is desirable for the candidate to have experience with the requirements of current Good Manufacturing & Documentation Practices in medical devices/pharma manufacturing facilities.
- Be able to work flexible hours in a dynamic environment with minimal direct supervision. Ability to work some Saturdays is required.
- *** The candidate must not be allergic to penicillin or cephalosporin drugs ***
- Basic science, math, and computer skills (including Microsoft Word and Excel) are required.
- Good writing, verbal communication, and problem-solving skills are required.
- Ability to work in a team environment and make independent decisions based on procedural and regulatory requirements.
- It is desirable for the candidate to have experience with the requirements of current Good Manufacturing & Documentation Practices in pharma manufacturing facilities.
- The candidate must be able to work flexible hours in a dynamic environment with minimal direct supervision.
- The ability to work on some weekends is required.
- Will work in both Drug Delivery and Penicillin facilities as needed.
- Overtime may be required to meet the production schedule.
skills: MS-EXCEL, Good Manufacturing Practices (GMP), Good Documentation Practices (GDP)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [email protected].
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
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