Biopharma Manufacturing Associate — Cleanroom & cGMP

ASK Consulting; Bothell (WA); On-site; USD 42,000 - 65,000; Full time

Job summary

ASK Consulting in Bothell, WA is seeking a Manufacturing Associate to support production in a cellular therapeutic manufacturing environment. The role emphasizes precise, timely completion of tasks and strict GMP adherence within a cleanroom setting.

Ideal candidates hold a life sciences degree or associates with related experience and have 0–2 years of cGMP manufacturing exposure. Local residency required; shift options include day or night schedules.

Qualifications

• Bachelor's or Associates in life sciences preferred; high school diploma with related experience accepted.
• 0-2 years of cGMP manufacturing experience desired.
• Proficiency with common office software and web-based tools; strong attention to detail and accountability.

Responsibilities

• Perform routine manufacturing tasks per written procedures and recognize deviations.
• Adhere to GMPs and standard operating procedures (SOPs).
• Weigh and verify raw materials; assemble, clean and sanitize equipment; monitor processes.
• Maintain cleanroom conditions to regulatory standards and complete work instructions.
• Train for proficiency on primary production equipment and process systems (e.g., Syncade MES, Oracle interfaces).
• Assist in revising process documents and SOPs; support inventory management.
• Support a safe work environment and collaborate with cross-functional manufacturing teams.
• Share batch information across teams and resolve routine production issues.

Skills

cGMP experience

Regulatory controlled environments

Attention to detail

Education

Bachelor's degree in Life Sciences

Job description

ASK Consulting in Bothell, WA is seeking a Manufacturing Associate to support production in a cellular therapeutic manufacturing environment. The role emphasizes precise, timely completion of tasks and strict GMP adherence within a cleanroom setting.

Ideal candidates hold a life sciences degree or associates with related experience and have 0–2 years of cGMP manufacturing exposure. Local residency required; shift options include day or night schedules.