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Manager/Sr. Manager, Quality Control

Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. As a global leader in the biology of the transforming growth factor beta (TGFβ) superfamily of cell proteins and named for the visual resemblance of a scholar rock to protein structures, the clinical-stage company is focused on advancing innovative treatments where protein growth factors are fundamental. Over the past decade, the company has created a pipeline with the potential to advance the standard of care for neuromuscular disease, cardiometabolic disorders, cancer, and other conditions where growth factor-targeted drugs can play a transformational role.

 

Scholar Rock is the only company to show clinical proof of concept for a muscle-targeted treatment in spinal muscular atrophy (SMA). This commitment to unlocking fundamentally different therapeutic approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. By harnessing cutting-edge science in disease spaces that are historically under-addressed through traditional therapies, Scholar Rock works every day to create new possibilities for patients. Learn more about the company’s approach at ScholarRock.com and follow @ScholarRock and on LinkedIn.


Summary of Position:


Scholar Rock is seeking an enthusiastic and highly motivated Manager/Senior Manager, Quality Control.  The role of Manager/Sr. Manager, Quality Control will be integral to the growing QC function at Scholar Rock as the programs progress from the R&D to cGMP stage, readying for commercialization and beyond.  The successful candidate will be responsible for: helping to define, communicate and implement the company’s quality control strategy and vision as part of the QC team. This role will utilize strong relationships to collaborate and interact with our development, clinical and operations teams to accomplish the company’s objectives. This individual will also collaborate and develop strong relationships with external CTL’s/CMO to ensure the appropriate testing, systems, processes, and activities are in place for Scholar Rock’s products. The successful candidate will utilize strong communication and relationship building skills to oversee Quality Control functions through external services.


A successful candidate will possess experience in analytical CMC, and potentially including interactions with the FDA and other agencies. Experience interacting with and managing external resources (CTO’s/CMO’s) is required. Ability to exert influence diplomatically and have a positive impact inside and outside of the organization. Demonstrated interpersonal, organizational, negotiation and communication skills. Excellent oral and written communication skills and computer skills. Ability to travel as needed.



Position Responsibilities
  • Review CTL/CMO’s tests raw data and make sure that tests are done in accordance with approved SOPs and results interpretation is correct
  • Manage and analyze the stability programs of the GMP DS, the GMP DP and the development (shelf extension) DS/DP and write periodic Technical Reports.  Rapidly informs and updates appropriate teams of OOT and OOS data.
  • Work with collaboration partners to ensure project deliverables 
  • Oversee CTL/CMO analysis documents, validations, and batch records 
  • Provide analytical support and input to developmental studies and issues during product development to ensure quality upon QC transfer/transition to commercial-readiness
  • Author/review department SOPs


Candidate Requirements
  • Bachelor’s Degree in appropriate scientific field with 8+ years of experience, or equivalent combination of experience and advanced degree
  • Knowledge of regulatory guidelines (GxP, FDA, ICH, EU, etc.).  Focus on biologics is a plus. 
  • Excellent writing and communication skills
  • Experience overseeing QC laboratory functions performed by a third-party CDMO or CTL
  • Strong technical analytical background


Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees

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Average salary estimate

$105000 / YEARLY (est.)
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$90000K
$120000K

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What You Should Know About Manager/Sr. Manager, Quality Control, Scholar Rock

If you’re looking to make a transformative impact in the biopharmaceutical industry, Scholar Rock has the perfect opportunity for you as Manager/Senior Manager, Quality Control based in Cambridge, MA! In this integral role, you’ll lead the charge to establish and execute the company's quality control strategy, particularly as our groundbreaking programs transition from research to commercialization. Collaborating closely with our talented development, clinical, and operations teams, you’ll be at the forefront of driving quality assurance while building strong relationships with external partners like CTL’s and CMO’s. Your responsibilities will involve reviewing raw test data, managing stability programs for GMP drug substances and products, and providing analytical support to ensure our offerings meet the most stringent standards. With your solid experience in analytical chemistry and quality control functions, you’ll effectively influence stakeholders and ensure compliance with regulatory guidelines. Scholar Rock thrives on innovation and creativity, and we value excellent communication and organizational skills, allowing you to share your insights and maintain a collaborative atmosphere. This is not just a role; it’s a chance to be part of a mission-driven company committed to creating life-changing therapies for conditions that have historically been under-addressed. If you’re passionate about leveraging your skills in a dynamic biopharmaceutical environment, we want to hear from you!

Frequently Asked Questions (FAQs) for Manager/Sr. Manager, Quality Control Role at Scholar Rock
What are the primary responsibilities of the Manager/Sr. Manager, Quality Control at Scholar Rock?

As the Manager/Sr. Manager, Quality Control at Scholar Rock, your primary responsibilities will include implementing the company's quality control strategy, managing the quality control operations as programs transition from research to cGMP production, and collaborating with both internal teams and external partners. You will ensure that all quality control testing aligns with approved SOPs and regulatory guidelines while also supervising analytical programs related to stability for drug substances and products.

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What qualifications are needed for the Manager/Sr. Manager, Quality Control position at Scholar Rock?

The ideal candidate for the Manager/Sr. Manager, Quality Control position at Scholar Rock should hold a Bachelor's Degree in a relevant scientific field, complemented by at least 8 years of experience in quality control. An advanced degree is a plus. You should be well-versed in regulatory guidelines such as GxP, FDA, and ICH, with a strong focus on biologics being advantageous. Additionally, excellent communication and interpersonal skills are essential for this role.

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How does the Manager/Sr. Manager, Quality Control interact with external CTL's and CMO's at Scholar Rock?

In the role of Manager/Sr. Manager, Quality Control at Scholar Rock, you will interact closely with external CTL’s and CMO’s to ensure that quality control testing and processes meet company standards. This collaboration involves oversight of testing procedures, validation of processes, and managing documentation to ensure compliance and uphold the highest quality throughout product development.

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What is the focus of quality control at Scholar Rock?

Quality control at Scholar Rock is centered on ensuring the safety and efficacy of our innovative therapies, particularly as we advance treatments for serious diseases. As a Manager/Sr. Manager, you will play a pivotal role in overseeing quality through comprehensive testing and stability programs, ensuring that every product meets established quality standards and regulatory requirements, which is essential for successful commercialization.

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What type of experience is beneficial for the Manager/Sr. Manager, Quality Control role at Scholar Rock?

Candidates seeking the Manager/Sr. Manager, Quality Control role at Scholar Rock will benefit from experience in analytical chemistry and good manufacturing practices (GMP). Familiarity with interactions involving the FDA and other regulatory bodies is strongly preferred, along with prior experience working with third-party organizations to oversee lab functions. Strong technical analytical skills and the ability to influence and communicate effectively are also crucial for success in this role.

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Common Interview Questions for Manager/Sr. Manager, Quality Control
Can you describe your experience with GMP quality control processes?

In answering this question, focus on specific protocols you've implemented in previous roles, emphasizing your understanding of GMP standards. Discuss any direct involvement with audits or compliance checks, highlighting how you ensured quality and regulatory adherence.

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How do you approach collaboration with external partners in quality control?

Share a specific example of how you successfully collaborated with external labs or organizations. Highlight the strategies you used to communicate effectively, resolve conflicts, and ensure that project goals were met, underscoring the importance of teamwork in achieving quality goals.

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What strategies do you use to stay updated on regulatory requirements?

In your response, mention resources you rely on, such as regulatory agency websites, professional webinars, and industry publications. Highlight the importance of continuous learning in maintaining compliance and implementing best practices within your team.

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How do you handle out-of-specification (OOS) results?

Explain the step-by-step process you follow for investigating OOS results. Emphasize the importance of thorough documentation, root cause analysis, and developing corrective actions to address issues while ensuring quality standards are maintained.

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Describe a challenging quality control issue you faced and how you resolved it.

Provide a real-life example that showcases your problem-solving skills. Detail the context of the issue, the steps you took to resolve it, and the impact your actions had on maintaining quality and compliance. This demonstrates your critical thinking and leadership capabilities.

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What quality control metrics have you used in previous roles?

Discuss specific metrics such as defect rates, test yield, or compliance rates. Explain how you used these metrics to identify improvements, set benchmarks, and enhance quality control processes within your team or organization.

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How do you prioritize tasks in a fast-paced quality control environment?

Describe your method for prioritizing based on urgency and impact on overall quality. Mention tools or systems you use for task management and how you communicate priorities with your team to ensure smooth operations and compliance.

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What do you believe is the role of a Quality Control Manager in team dynamics?

Discuss how a Quality Control Manager contributes to fostering a culture of quality and collaboration. Emphasize the importance of providing guidance, support, and training to team members to promote engagement and alignment with quality objectives.

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Can you give an example of how you’ve influenced cross-functional teams?

Share a situation where you successfully influenced a cross-functional team to prioritize quality. Highlight specific communication strategies you employed and the resulting positive changes or outcomes that emphasized quality control.

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How do you ensure compliance with quality standards during product development?

Explain your approach to embedding quality practices throughout the product lifecycle, from initial development to final testing. Discuss early engagement with teams, regular reviews, and continuous training to uphold compliance with quality and regulatory standards.

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Relentlessly focused on seeing new possibilities in deep structural insights, validated biologies and antibody technologies to allow us to move with speed and urgency to deliver high-impact medicines to patients with devastating diseases.

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DATE POSTED
December 4, 2024

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