mcs manufacturing sr. associate.

• newbury park , california

• posted august 19, 2024

job details

summary

• $30 - $37.44 per hour

• contract

• postgraduate degree

• category life, physical, and social science occupations

• reference48716

job details

job summary:

As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!

location: Newbury Park, California

job type: Contract

salary: $30.00 - 37.44 per hour

work hours: 9 to 5

education: Masters

responsibilities:

• Change control ownership, ensuring records are comprehensive and compliant per GMP regulatory procedures. This must occur with a Right the First-Time approach.

• Strong project management skills, with prior project experience preferred.

• Timely closure of change control records in relation to procedural guidance and/or disposition timelines

• Represent Building 20 Manufacturing as the receiving site for incoming Technology Transfers/New Product Introductions into Building 20

• Identifying improvement opportunities within the organization and take pro-active steps to build consensus to implement those opportunities

• Succinctly communicate verbally and in writing to staff and leadership

• Presenting records and business processes to a variety of audiences, including auditors and inspectors

• Participating/leading Continuous Improvement Transformation activities

• Champion safety and compliance at all times

qualifications:

• Master's Degree

• Experience with PAS X Werum software for electronic batch records

• Technical understanding of Drug Product (DP) manufacturing operations, such as buffer batching, DP formulation, DP Filling, Inspection

• Experience leading change controls in Trackwise

• Degree in life sciences or engineering

• Strong scientific, technical interactions with partner organizations such as Process Development, Process Engineering, Supply Chain, Quality Control, Regulatory

• Demonstrated technical writing skill

• Demonstrated ability to work in a team

skills: Quality control, SOP, GMP (Good Manufacturing Practice), Clinical Supply Chain

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.

Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.

We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.