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document control specialist.

• fort worth , texas

• posted october 2, 2024

job details

summary

• $25 - $28 per hour

• contract

• bachelor degree

• category life, physical, and social science occupations

• reference49075

job details

job summary:

Randstad is the #1 HR Services Company in the World and we are sourcing for a Document Control Specialist in the Dallas / Fort Worth, TX area. The ideal candidate will have 1 to 2 years of experience in a similar role creating and revising GMP manufacturing batch records, investigations, and change controls. If they have experience on liquid and solid dose manufacturing that would be a huge plus. This is a contract role and can start immediately.

location: Fort Worth, Texas

job type: Contract

salary: $25 - 28 per hour

work hours: 8 to 4

education: Bachelors

responsibilities:

Essential Functions

• Interact with technical associates, leads and subject matter experts (SMEs) from other departments and divisions to create and revise GMP Manufacturing Batch Records, investigations, and change controls with a strong emphasis on liquid and solid dose manufacturing and packaging.

• Prepare, write, update, and maintain manufacturing batch records, SOPs and FORMs where applicable, including the preparation of any forms or attachments that may accompany the SOP.

• Other duties as assigned.

qualifications:

Required Core Competencies:

• Effective skills in all areas of communication, collaboration, and decision-making.

• Great attention to detail with the ability to work on multiple projects.

• Work effectively with minimal supervision / independently with a sense of urgency.

• Must be able to articulate their ideas clearly and concisely through effective written communication.

• Must meet deadlines.

• Strong organizational skills are essential, with a proven ability to manage and track multiple projects simultaneously while adapting to shifting priorities.

• Ability to follow up with multiple departments is required.

• Ability to create standard operating procedures as well as other supporting documentation, as needed.

Minimum Education/ Experience:

• Degree (BA/BS) in a technology-related field (Biology, Chemistry, Pharmacy, Engineering, etc.).

• At least 2-5 years of technical writing experience years in a cGMP manufacturing environment.

• Strong command of the English language is essential. Ability to accurately convey information in both spoken and written form.

• Computer experience required. Proficiency in Microsoft Office (Word, Excel, and Outlook) is a must.

skills: Editing, NDA, Administration, Office Management, Biology, Chemistry, System Administration, Safety Narrative, Biostatistical Analysis, GMP (Good Manufacturing Practice), QC Review

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 HRsupport@randstadusa.com.

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 health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

This posting is open for thirty (30) days.