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Job Title: Documentation Specialist

Job Description

Join a leading global bio-pharmaceutical manufacturing organization as a Documentation Specialist in the quality team. This role involves preparing and reviewing essential documentation for the QC lab and implementing change control processes using the Global Quality Tracking System (QTS) and PDOCs.

Responsibilities

+ Consistently adhere to company, site, and laboratory safety rules and promptly report any safety issues.

+ Follow procedures at all times, adopting cGMP and cGDP practices.

+ Edit and write Standard Operating Procedures and other documentation as needed.

+ Initiate and facilitate change requests in PDOCS and the Global Quality Tracking System (QTS).

+ Reconcile change requests from initiation to closure.

+ Review and approve documents in the change control system.

Essential Skills

+ Bachelor’s degree with 1 to 2 years of experience in a controlled document management/records management position.

+ Thorough knowledge of cGMP and cGDP.

+ Proficient in Microsoft Office (Word, Excel, PowerPoint).

+ Ability to work independently and multi-task in a fast, priority-switching environment.

+ Strong attention to detail and excellent written and verbal communication skills.

+ Strong reading comprehension and proofreading skills.

+ Strong organizational skills.

+ Demonstrated ability to work and contribute in a team-based environment.

+ Team and customer oriented.

+ Ability to facilitate process improvements.

Additional Skills & Qualifications

+ Experience in chemistry is ideal.

+ Technical writing skills.

Work Environment

The role is primarily desk-based with significant time spent on the computer. It involves interaction with QC lab analysts, managers, supervisors, and SMEs within QC. The work schedule is Monday to Friday, starting between 7-9 am, for 8 hours a day. The on-site work is rotational with 2.5 days on-site and flexibility for remote work if preferred. Candidates must be willing to work on-site up to 5 days a week if business needs require.

Job Type & Location

This is a Contract to Hire position based out of Rocky Mount, NC.

Pay and Benefits

The pay range for this position is $25.00 - $43.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Rocky Mount,NC.

Application Deadline

This position is anticipated to close on Dec 31, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.