Quality Assurance Specialist

Astrix; Brownsburg (IN); On-site; USD 70,000 - 75,000; Full time

Job summary

Join a dynamic team at a leading Biotech company as a Quality Assurance Specialist! This exciting role offers the chance to ensure compliance and quality in the production of life sciences products. With a focus on reviewing documentation and inspecting materials, you'll play a crucial part in maintaining high standards in a fast-paced environment. The company values your growth and success, providing a supportive atmosphere for professionals eager to make a difference in the pharmaceutical industry. If you have a passion for quality assurance and a background in life sciences, this is the perfect opportunity for you!

Benefits

Medical/dental coverage

Weekly pay

401k and PTO after 6 months

Great benefit package upon conversion

Qualifications

• 3+ years of Quality Assurance experience in the life sciences.
• Strong understanding of GMP and related documentation.

Responsibilities

• Review production batch records and ensure compliance with SOPs.
• Inspect and release incoming raw materials and packaging components.

Skills

Quality Assurance

GMP experience

Life Sciences knowledge

Education

B.S. degree in Life Sciences

Job description

This range is provided by Astrix. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$70,000.00/yr - $75,000.00/yr

Join our amazing team! We want to help you continue to succeed and grow in the life sciences industry!

Our Quality Assurance Specialist position is a great opportunity to work with a leading Biotech company!

We are looking for a sharp professional that possesses these top 3 skills:

• B.S. degree in the life sciences
• 3+ years of QA experience
• Experience in the pharmaceutical, biologic, medical device, or radiopharma industry

Schedule: 2nd shift- 3p-11p* (flexibility required for 1st or 3rd shift as well)

Type of Job: C2H; possibly Direct Hire

Location: (Onsite- Brownsburg, IN)

At this time, Astrix cannot transfer nor sponsor a work Visa for this position.

Relocation assistance is not available for this position.

Benefits Offered:

• Medical/dental coverage!
• Weekly pay!
• 401k and PTO after 6 months!
• Great benefit package offered upon conversion!

Quality Assurance Specialist Daily Tasks:

• Review production batch records, logbooks, and associated documentation to assess completeness, accuracy, and compliance with SOPs.
• Inspect, review documentation, and release incoming raw materials and packaging components, as needed.
• Follow up on investigations and deviations related to manufacturing activities.
• Scan batch record documentation such as batch records, raw materials, investigations, and deviations.
• Review of equipment and instrumentation documentation in support of GMP manufacturing and testing operations.

Quality Assurance Specialist Qualifications/Requirements:

• B.S. degree in the Life Sciences required
• 3+ years of GMP experience from any of the following industries (Pharmaceutical, biologics, Medical device, radiopharma)
• 3+ years of Quality Assurance experience

We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Seniority level

Associate

Employment type

Full-time

Job function

Quality Assurance

Industries

Pharmaceutical Manufacturing