Our client is seeking a dedicated and detail-oriented Central Services Technician to join their team.

Job Posting:

Job title: Central Services Technician I

Duration: 3 months

Shift timings: 7pm - 7am (2-2-3 rotation)

Overview:

We are seeking a detail-oriented and motivated individual to join our team as a Central Services Technician I. In this role, you will support GMP manufacturing batch records execution and ensure necessary supply levels in manufacturing areas. You will contribute to the overall GMP manufacturing process through the application of operational knowledge in the production of bulk products from microbial and cell culture systems.

Key Responsibilities:

Execute manufacturing batch records, SMPs, work instructions, and/or SOPs with a focus on proactive, right-the-first-time execution.

Document all activities to meet cGMP requirements.

Operate central services processing equipment per established SOPs, including biological safety cabinets, mixers, autoclaves, washers, balances/scales, and pH/conductivity meters.

Identify and support the implementation of Continuous Improvement opportunities.

Recognize waste within work processes and identify cost-saving projects or initiatives.

Adhere to all cGMPs, compliance/regulatory mandates, and quality requirements.

Review daily GMP documentation for accuracy and completeness (e.g., logbooks, SMPs, batch records).

Qualifications:

High school diploma or GED required.

1-2 years' experience working in a GMP facility preferred (reduced experience considered with higher education in an applicable discipline).

Strong communication skills.

Basic computer skills, including proficiency in Microsoft Office.

Ability to lift up to 25 lbs.

Flexibility, adaptability, self-motivation, and a strong work ethic.

Ability to work independently and collaborate effectively across teams and partners.

Familiarity with lean, action-oriented organizations is a plus.

Additional Requirements:

Commitment to adhering to all company policies, compliance requirements, and quality standards.

Perform other related duties as assigned to support departmental and company objectives.

If you are a dedicated professional looking for a challenging and rewarding opportunity in GMP manufacturing, we encourage you to apply.

If this is a role that interests you and you’d like to learn more, click apply now and a recruiter will be in touch with you to discuss this great opportunity. We look forward to speaking with you!

About ManpowerGroup, Parent Company of: Manpower, Experis, Talent Solutions, and Jefferson Wells

ManpowerGroup® (NYSE: MAN), the leading global workforce solutions company, helps organizations transform in a fast-changing world of work by sourcing, assessing, developing, and managing the talent that enables them to win. We develop innovative solutions for hundreds of thousands of organizations every year, providing them with skilled talent while finding meaningful, sustainable employment for millions of people across a wide range of industries and skills. Our expert family of brands – Manpower, Experis, Talent Solutions, and Jefferson Wells – creates substantial value for candidates and clients across more than 75 countries and territories and has done so for over 70 years. We are recognized consistently for our diversity - as a best place to work for Women, Inclusion, Equality and Disability and in 2022 ManpowerGroup was named one of the World's Most Ethical Companies for the 13th year - all confirming our position as the brand of choice for in-demand talent.

ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.