Associate Director, Quality Control (56861)

Praxis Precision Medicines Inc.; Boston (MA); Remote; USD 150,000 - 169,000; Full time

Job summary

An innovative biopharmaceutical company is seeking a highly experienced Associate Director for Quality Control to lead critical quality activities in product testing and release. This role involves overseeing compliance with GMP standards and managing quality control for both clinical and commercial products. As part of a dynamic team, you will play a pivotal role in ensuring the integrity of product development, while also contributing to a culture of trust and curiosity. With a comprehensive benefits package and opportunities for growth, this position offers a chance to make a significant impact in the field of central nervous system therapies.

Benefits

99% premium cost covered for medical, dental, and vision

Bonus program

401k plan with 100% match

Wellness benefit of $200/month

Unlimited PTO

Equity awards eligibility

Employee Stock Purchase Plan

Qualifications

• 6+ years of experience in cGMP Quality Control environment required.
• In-depth understanding of GMP biologics manufacturing and testing.

Responsibilities

• Oversee quality control of contract lab activities and testing results.
• Manage compliance for stability and reference standard programs.

Skills

cGMP Quality Control

Regulatory Compliance

Analytical Method Validation

Communication Skills

Project Management

Education

Bachelor's Degree

Tools

Quality Control Systems

Stability Testing

Certificate of Analysis Generation

Job description

Job Details

Job Location: Remote - Boston, MA

Position Type: Full Time

Education Level: 4 Year Degree

Salary Range: Undisclosed

Travel Percentage: Minimum of 2x/year to Boston area

Job Category: Biotech

Associate Director, Quality Control

Reports to: Senior Director, Quality Operations, CMC
Location: This position may be performed remotely with travel to the Boston area as needed.

Position Summary

Praxis is seeking a highly experienced, motivated, and innovative quality leader with strong experience in late-stage development and commercialization to join our Quality team as Associate Director, Quality Control to support QC product release and stability activities. Reporting to Senior Director, Quality Operations CMC, this position will be responsible for managing and executing Quality Control activities in support of product testing, release, and stability, and toxicology studies test material inventory support. Ensure GMP activities are conducted in accordance with applicable SOPs, compendia, approved methods, and in accordance with company’s and regulatory agencies’ policies and procedures.

Primary Responsibilities

• Quality control oversight of contract lab activities e.g. routine testing, testing results review and approval, generation of Certificate of Analysis, review/approval of technical documents such as method validation and qualification protocols/reports, and regulatory filing documents per project needs as required.
• Manage and lead clinical and commercial quality control compliance for stability, reference standard, and specification programs.
• Support the establishment of QC systems such as product specifications, product expiry, reference standard program, QC documentation including SOPs, material specifications and other quality documents, etc.
• Support CMC Analytical Development in a QC aspect by review and approval of applicable documents in support of activities such as method development, transfer, characterization, comparability investigations, analytical test method qualification plans/protocols and reports.
• Perform data review of trending for in-process testing, release, and stability and identify data trends, to ensure compliance with regulatory filings and ICH or other global health authority guidance documents, as applicable.
• Support technology transfer and process performance qualification with product characterization/process validation activities.
• QC support in the generation, quality, and compliance review of bioanalytical data from preclinical and clinical projects for proprietary compounds and in some cases support for sample analysis projects.
• Support tox material inventory monitoring process, to ensure no impediments to completing studies.
• Additional responsibilities and ad hoc projects as required.

Qualifications and Key Success Factors

• Bachelors degree strongly preferred, with minimum of 6 years of experience in cGMP Quality Control environment.
• In-depth technical and regulatory understanding of GMP biologics manufacturing and testing including applicable international regulations/standards (GMP and ICH guidelines) in all phases of product development and commercialization.
• Experience managing third party assay laboratories, collaborations, and relevant bioanalytical vendors preferred.
• Extensive knowledge of GMP regulations, ICH guidelines, and stability testing requirements.
• Proven track record of managing stability programs and COA processes for clinical and commercial products.
• Experience working in QC lab environment with hands-on experience in running, qualifying, and validating analytical methods.
• Ability to work effectively in a fast-paced, dynamic environment.
• Experience managing Contract Test Labs activities.
• Experience with regulatory inspections and interactions with health authorities.
• Excellent communication skills and ability to build key networks and business relationships across all levels of the business.

Compensation & Benefits

At Praxis, we’re proud to offer an exceptional benefits package that includes:

• 99% premium cost covered for medical (Blue Cross Blue Shield), dental, and vision plans.
• Bonus program structured to pay on a quarterly basis.
• 401k plan with 100% match up to 6% of employee’s contribution (Traditional & Roth).
• Wellness benefit of $200/month towards incredibly flexible options including travel, fitness equipment & memberships, student loan repayment, sports fees and much more.
• Unlimited PTO, (2) weeklong shutdowns each year, and a generous extended family leave benefit.
• Eligibility for equity awards and Employee Stock Purchase Plan (15% discount).

To round out this world-class total rewards package, we provide base salary compensation in the range of $150,000 to $169,000 annualized. Final salary range may be modified commensurate with job level, education, and experience.

Company Overview

Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders characterized by neuronal imbalance. At Praxis we share a common vision of reshaping the human condition into a more freeing and fulfilled existence by developing high impact medicines for patients and families affected by and living with complex brain disorders. Our core Values of Trust, Ownership, Curiosity and Results are foundational to every aspect of our business and are exemplified by each and every one of our team members.

Diversity, Equity & Inclusion

Guided by our core values, at Praxis Precision Medicines, Inc. we continue to DARE FOR MORE to advance, promote, and champion diversity, equity, and inclusion by encouraging individuals to bring their authentic selves and perspectives to work each day. We are an equal opportunity employer and committed to providing opportunities to all qualified applicants without regard to race, religious creed, color, gender identity or expression, age, national origin, sexual orientation, disability, genetics, military service and veteran status, or any other characteristic protected by federal, state, or local laws.