MCS Associate Quality Control

Aditi Consulting; Thousand Oaks (CA); On-site; USD 28,929 - 31,684; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

401(k) plan participation

10 paid days off

Commuter benefits

Life and disability insurance

Job summary

An established industry player in pharmaceutical manufacturing is seeking a dedicated Quality Assurance Associate. This role involves performing routine laboratory procedures, conducting analytical testing, and ensuring compliance with safety guidelines and regulatory requirements. Ideal candidates will demonstrate strong communication skills, attention to detail, and the ability to manage multiple priorities in a dynamic environment. Join a team that values flexibility and continuous improvement while contributing to vital research and manufacturing processes in biotechnology. This is an exciting opportunity to grow your career in a supportive and innovative setting.

Qualifications

• Must learn and comply with safety guidelines and cGMPs.
• Ability to adhere to regulatory requirements and written procedures.

Responsibilities

• Perform routine laboratory procedures and analytical testing.
• Document, compute, compile, interpret, and enter data.

Skills

Analytical testing experience

GMP/GDP knowledge/experience

Strong written and oral communication skills

Detail-oriented

Ability to organize work

Ability to evaluate documentation/data

Flexibility and adaptability

Job description

Shift/Schedule: 8:30 - 5:30 pm (flex by an hour)

Job Description:

• Under general supervision, this position will perform routine procedures and testing in support of the lab.
• This position will be responsible for one or more of the following activities: - Performing routine laboratory procedures - Routine analytical testing - Documenting, computing, compiling, interpreting, and entering data - Maintaining and operating specialized equipment - Initiating and/or implementing changes in controlled documents.
• Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory logbooks.

Preferred Qualifications:

• Ability to adhere to regulatory requirements, written procedures and safety guidelines
• Ability to evaluate documentation/data according to company and regulatory guidelines
• Ability to organize work, handle multiple priorities and meet deadlines
• Strong written and oral communication skills
• Must be detail oriented
• Must be flexible and adaptable to changing priorities and requirements
• Demonstrate understanding of regulatory requirements, safety guidelines and factors impacting compliance
• Demonstrates understanding of when and how to appropriately escalate.
• May identify, recommend and implement improvements related to routine job functions.
• Must learn and comply with safety guidelines and cGMPs.

Top 3 Must Have Skill Sets:

• Analytical testing experience
• GMP/GDP knowledge/experience

Pay Transparency:

The typical base pay for this role across the U.S. is: $21.00 - $ 23.00 /hr. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience and the benefits package you select. Full-time employees are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, 10 paid days off, 401(k) plan participation, commuter benefits and life and disability insurance.

Seniority level:

Associate

Employment type:

Contract

Job function:

Quality Assurance

Industries:

Pharmaceutical Manufacturing and Biotechnology Research