quality assurance senior specialist.

• newbury park , california (remote)

• posted october 16, 2024

job details

summary

• $35 - $40.81 per hour

• contract

• bachelor degree

• category life, physical, and social science occupations

• reference49165

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: Telecommute

job type: Contract

salary: $35.00 - 40.81 per hour

work hours: 9 to 5

education: Bachelors

responsibilities:

• Coordinate Global Incoming Quality Process Operations to support Global Process Owner lead. Interface with IQA Network, various Company sites and business partners to ensure maintain process in compliance and alignment.

• Complete and approve multisite procedures, deviation, change control, SAP master data record and other quality records to support RM Network.

• Candidate must have strong leadership skills, communication skills, and the ability to approach issues from a strategic perspective.

• Ensure operations align with applicable regulations and Company requirements relating to Good Manufacturing Practices, Good Distribution Practices, Good Documentation Practices, and safety.

• Understand and incorporate risk management strategy into overall IQA process operation.

• Represent the IQA Network during audits and inspections and directly interact with inspectors as requested. Perform Quality Assurance assessments for IQA global operation (i.e., new material specifications, new or revise physical methods and multisite procedures revision).

• This includes the ability to translate strategy into challenging, actionable objectives to effectively drive your team, advocate client positions throughout the life cycle of the project and make value-based decisions.

qualifications:

• Requirements: Bachelor's Degree in Life Sciences or related field or the equivalent combination of education and/or experience.

• Typically 2 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry.

• Evaluate documentation and operation and documentation according to company guidelines.

• Be self motivated, attentive to details and able to prioritize and meet deadlines.

• Basic statistical mathematical skills including the ability to trend data.

• Basic project management skills. Independently understand, follow and implement instructions.

• Strong word processing, database and spreadsheet application skills.

• Strong organizational skills with the ability to manage multiple projects or assignments.

skills: Quality Assurance, GMP (Good Manufacturing Practice)

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.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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

Qualified applicants in the unincorporated areas of Los Angeles County with criminal histories will be considered for employment in accordance with the Los Angeles County's Fair Chance Ordinance for Employers.

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.