Lab Manufacturing Associate II

Pride Global; Bothell (WA); On-site; USD 62,000 - 73,000; Full time

Benefits offered by this job

Healthcare coverage

401(k) retirement savings

Life & disability insurance

Employee discounts

Job summary

PrideGlobal is seeking a Manufacturing Associate II to join our team near Bothell, WA. You will execute manufacturing processes safely and on schedule, following cGMP and SOPs, and maintain accurate GMP documentation.

The ideal candidate will have a Bachelor's degree in a scientific field and at least 2 years of GMP biopharmaceutical manufacturing experience, with familiarity in cell therapy or bioprocessing being a plus. This is a 3-month contract position with potential extension.

Qualifications

• Bachelor's degree in a related scientific field.
• Minimum 2 years of GMP biopharmaceutical manufacturing experience.
• Experience with cell therapy, mammalian cell culture, microbial fermentation, viral vectors, or plasmid manufacturing preferred.
• Knowledge of deviations, CAPAs, change management, and quality management systems (QMS).
• Experience with MES, ERP, or electronic batch record systems.

Responsibilities

• Execute manufacturing processes safely, accurately, and according to production schedules.
• Follow cGMP, SOPs, batch records, and safety procedures.
• Complete and review GMP documentation accurately and on time.
• Perform equipment maintenance, calibration, cleaning, and routine facility activities.
• Support inventory management and daily manufacturing operations.
• Escalate manufacturing issues and deviations to management and Quality Assurance.
• Collaborate effectively with Manufacturing, Quality, and other cross-functional teams.

Skills

GMP manufacturing

Documentation accuracy

Cross-functional collaboration

Safety compliance

Education

Bachelor's degree in Biochemistry/Bioengineering/Chemical Engineering/Biology

Tools

MES

ERP

Electronic batch records

Job description

Russell Tobin is partnering with a pharmaceutical company to identify a Manufacturing Associate II for an opportunity near Bothell, WA.

Key Responsibilities

• Execute manufacturing processes safely, accurately, and according to production schedules.
• Follow cGMP, SOPs, batch records, and safety procedures.
• Complete and review GMP documentation accurately and on time.
• Perform equipment maintenance, calibration, cleaning, and routine facility activities.
• Support inventory management and daily manufacturing operations.
• Escalate manufacturing issues and deviations to management and Quality Assurance.
• Collaborate effectively with Manufacturing, Quality, and other cross-functional teams.

Required Qualifications

• Bachelor's degree in Biochemistry, Bioengineering, Chemical Engineering, Biotechnology, Biology, or a related scientific field.
• Minimum 2 years of GMP biopharmaceutical manufacturing experience.
• Experience with cell therapy, mammalian cell culture, microbial fermentation, viral vectors, or plasmid manufacturing preferred.
• Knowledge of deviations, CAPAs, change management, and quality management systems (QMS).
• Experience with MES, ERP, or electronic batch record systems.

Additional Details

• Location model: Bothell, WA
• Position Type: 3 months contract with potential for extension
• Pay range approved: $30-$35/hr. depending on experience

Benefits

• For workers in the United States, PrideGlobal and it's affiliates offers eligible employee's comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), 401(k)-retirement savings, life & disability insurance, an employee assistance program, legal support, pet insurance and employee discounts with preferred vendors.

Only applicable for San Francisco Candidates

Under the San Francisco Lactation in the Workplace Ordinance, we will provide written notice of lactation accommodation rights, and this notice will automatically be given upon hiring, any inquiry of parental leave or lactation accommodation.

Equal Employment Opportunity

PrideGlobal and it's affiliates are an equal opportunity employer. We do not discriminate on the basis of the race, religious creed, color, national origin, ancestry, physical disability, mental disability, reproductive health decision making, medical condition, genetic information, marital status, sex, gender, gender identity, gender expression, age, sexual orientation, veteran or military status, or any other characteristic protected by applicable federal, state, or local law.

Fair Chance Employment

PrideGlobal and it's affiliates are a Fair Chance employer. We consider all qualified applicants, including those with criminal histories, in a manner consistent with applicable state and local Fair Chance laws and ordinances, including, the California Fair Chance Act and all applicable local Fair Chance ordinances.

Accommodations

We are committed to providing reasonable accommodations to applicants and employees with disabilities. If you require a reasonable accommodation to participate in the application or interview process, or to perform the essential functions of this role, please contact us.

Only applicable for Kentucky positions

For this type of employment, state law requires a criminal record check as a condition of employment. This applies to direct care staff (Examples: RN, LPN, Nurse Aides, Therapists) referred to Kentucky nursing facilities, assisted living communities, or long-term care facilities, in accordance with KRS 216.793.