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Sr. Quality Control Analyst

About Us

Pace Life Sciences

Pace makes the world a safer, healthier place. We advance the science of our pharmaceutical and biopharmaceutical customers through the drug development process, from early-phase R&D through clinical trials and GMP commercial product support. For customers with in-house manufacturing and labs, Pace provides professional services to support their operations.

Job Description SUMMARY

Responsible for providing or overseeing the analysis, administration and oversight of comprehensive chemistry/biochemistry policies, programs and practices; may provide feedback and guidance to clients regarding the analysis of materials, products and/or devices utilizing complex to specialized professional and technical knowledge of chemistry/biochemistry/formulation development or related equipment, testing, and procedures. May design and develop robust and scalable formulations for small molecules and biologics for early-stage clinical trials. May develop and optimize manufacturing processes for drug products. May interpret analytical data to guide formulation and process development decisions.

ESSENTIAL FUNCTIONS
  • Serves as a lead to staff to include providing work direction, guidance, and training.
  • Overseeing or reviewing, completing, and processing comprehensive types of forms, documents, databases, and related materials and information.
  • Provides complex to specialized analysis in support of various testing materials, products and/or devices utilizing various analytical instrumentation; follows Standard Operating Procedures and methods to perform testing.
  • Provides complex to specialized review, analysis, interpretation, and documentation of testing results. Analyzes and reviews complex to specialized operations, results, feedback, and related chemistry/biochemistry/formulation information on an as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management and/or clients.
  • Provides training and guidance on analytical tests, methods, and instrumentation, as required.
  • Provides complex to specialized analysis, interpretation and counsel to clients, staff, management, and functional leaders regarding chemistry/biochemistry policies, programs, and practices; involves broad operations and leading implementation and change.
  • Analyzes and reviews complex to specialized operations, results, feedback, and related chemistry/biochemistry/formulation information on an ongoing to as needed basis to determine trends, draw conclusions, interpret findings, and presents results, proposals, and recommendations to management and/or clients.
  • Assists with developing or participating in chemistry/biochemistry/formulation or cross functional project or program objectives, which includes proposed budgets, timelines, materials, personnel, and other project requirements, receives direction, and presents information to management and/or clients.
  • Develop validate and transfer analytical methods. Provide routine and non-routine analysis using instruments such as HPLC, GC, LC-MS, and FTIR, DD-PCR, among others.
  • Design and develop robust and scalable formulations for small molecules and biologics for early-stage clinical trials. May develop and optimize manufacturing processes for drug products.
  • Ensure all activities adhere to SOP's, regulatory guidelines, GLP and GMP standards.
  • Contributes to the efficiency and effectiveness of the department's service to its customers by offering suggestions and directing or participating as an active member of a work team.
  • Promotes and supports the overall mission of Pace Analytical by demonstrating courteous and cooperative behavior when interacting with customers and staff; acts in a manner that promotes a harmonious and effective workplace environment.
QUALIFICATIONS Education and Experience
  • Bachelor's degree in chemistry/biochemistry, or a closely related field.
  • Three to five (3-5) years of experience, including experience with specialized or technical programs or operations; OR an equivalent combination of education, training, and experience. Master's or PhD degree is strongly preferred.
Required Knowledge and Skills Required Knowledge
  • Complex to specialized principles, practices, and techniques of chemistry/biochemistry and formulation development.
  • Broad understanding of the administration and oversight of chemistry/biochemistry programs, policies, and procedures.
  • Complex to specialized methods to resolve chemistry/biochemistry problems, questions, and concerns.
  • Broad understanding of applicable chemistry/biochemistry laws, codes, and regulations.
  • Understanding of broad testing tools, equipment, and calibration.
  • Computer applications and systems related to the work.
  • Principles and practices to serving as an effective project team member.
  • Methods to communicate with staff, coworkers, and customers to ensure safe, effective, and appropriate operations.
  • Correct business English, including spelling, grammar, and punctuation.
Required Skills
  • Performing complex to specialized professional-level chemistry/biochemistry duties in a variety of assigned areas.
  • Overseeing and administering broad and varied chemistry/biochemistry/formulation functions.
  • Ability to operate and train others in analytical instruments and manufacturing equipment.
  • Training others in policies and procedures related to the work.
  • Serving as a team member and the development and management of projects.
  • Operating in a both a team and individual contributor environment.
  • Interpreting, applying, and explaining applicable laws, codes, and regulations.
  • Preparing advanced to expert functionals reports, correspondence, and other written materials.
  • Using initiative and independent judgment within established department guidelines.
  • Using tact, discretion, and prudence in working with those contacted during the work.
  • Performing effective oral presentations to large and small groups across functional peers and the department.
  • Contributing effectively to the accomplishment of team or work unit goals, objectives and activities.
  • Establishing and maintaining effective working relationships with various individuals contacted in the work.
Additional Information

Benefits

80 hrs of paid vacation per year, 7 paid holidays per year, 2 floating holidays per year (prorated based on start date), 40 hrs paid sick time per year, paid bereavement leave (days based on relation to the employee), 8 hrs paid volunteer time per year, parental leave, medical, dental, vision, voluntary short-term disability, long-term disability, life insurance, voluntary supplemental life insurance, traditional 401k and ROTH 401k with a company match, HSA, FSA, employee referral bonus, employee assistance program, tuition reimbursement program, employee recognition program, voluntary ID theft coverage, voluntary legal coverage, voluntary accident insurance, voluntary hospital indemnity insurance, and voluntary critical illness insurance.

Equal Opportunity Employer

Pace provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.


Work Schedule Monday-Friday, 8:00am-5:00pm

Average salary estimate

$80000 / YEARLY (est.)
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$70000K
$90000K

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What You Should Know About Sr. Quality Control Analyst, Pace Analytical

Join Pace Life Sciences as a Sr. Quality Control Analyst and make a meaningful impact in the world of pharmaceuticals and biopharmaceuticals! Situated in beautiful Middlesex County, MA, our company is committed to advancing science for our customers through every stage of drug development. In this role, you’ll harness your expertise in chemistry and biochemistry to oversee the analysis and adherence to comprehensive policies and programs. You will take charge of designing reliable and scalable formulations for both small molecules and biologics, playing a critical part in early-stage clinical trials. Your insights will be instrumental in interpreting analytical data and guiding formulation and process development decisions. As a leader, you’ll provide training, administration, and direction not only to your team but also to clients, ensuring that all operations comply with regulatory standards and best practices. You’ll collaborate in cross-functional projects, contribute to continuous improvements, and support a culture of cooperation and respect in the workplace. With a Bachelor’s degree in a relevant field and a few years of experience under your belt, you're not just filling a position but making a difference with Pace’s mission to create a safer, healthier world. If you’re ready to lead, innovate, and bring your analytical prowess to life, we’d love to hear from you!

Frequently Asked Questions (FAQs) for Sr. Quality Control Analyst Role at Pace Analytical
What are the essential responsibilities of a Sr. Quality Control Analyst at Pace Life Sciences?

The Sr. Quality Control Analyst at Pace Life Sciences is responsible for overseeing the analysis and administration of chemistry and biochemistry related policies. This role includes designing robust formulations for clinical trials, optimizing manufacturing processes, and interpreting data to guide development decisions. The Analyst also provides training and guidance to staff, ensures adherence to regulatory standards, and contributes to cross-functional projects.

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What qualifications are necessary to apply for the Sr. Quality Control Analyst role at Pace Life Sciences?

To qualify for the Sr. Quality Control Analyst position at Pace Life Sciences, candidates typically need a Bachelor’s degree in chemistry, biochemistry, or a closely related field. While three to five years of relevant experience are preferred, an advanced degree such as a Master’s or PhD is strongly preferred, underscoring the importance of specialized knowledge and skills for this role.

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What methods and instruments does the Sr. Quality Control Analyst use at Pace Life Sciences?

The Sr. Quality Control Analyst utilizes various analytical instrumentation such as HPLC, GC, LC-MS, FTIR, and DD-PCR to conduct complex analyses. Mastery of these instruments is crucial for interpreting results and developing quality control processes that adhere to the highest regulatory standards at Pace Life Sciences.

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How does the Sr. Quality Control Analyst contribute to team projects at Pace Life Sciences?

The Sr. Quality Control Analyst contributes significantly to team projects by providing complex analytical insights and developing project objectives, estimated budgets, and timelines. This role involves collaborating with various departments, ensuring that the chemistry and biochemistry perspectives align with overall project goals and contribute to successful outcomes.

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What does a typical work schedule look like for a Sr. Quality Control Analyst at Pace Life Sciences?

A typical work schedule for a Sr. Quality Control Analyst at Pace Life Sciences is Monday to Friday, from 8:00 am to 5:00 pm. This structured schedule allows for collaboration with team members and management while ensuring effective time management to meet project deadlines.

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Common Interview Questions for Sr. Quality Control Analyst
Can you describe your experience with analytical instrumentation relevant to the Sr. Quality Control Analyst position?

In your response, highlight specific instruments such as HPLC, GC, or LC-MS you’ve worked with, including the types of analyses performed and how those experiences relate to the responsibilities at Pace Life Sciences.

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How do you ensure that your work adheres to GMP and GLP standards?

Explain your process for maintaining compliance with GMP and GLP standards, including the specific practices you implement in testing and reporting to uphold regulatory requirements in your previous experiences.

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Describe a challenging project you worked on as a Quality Control Analyst and how you overcame obstacles.

Share a specific example where you faced challenges within a project, how you addressed them, your thought process, and the successful outcome. This showcases your problem-solving skills and resilience in the analytical field.

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What approaches do you take when leading and training a team in a Quality Control environment?

Discuss your leadership style and training methods. Emphasize how you foster a collaborative environment while sharing your expertise to enhance your team's capabilities in analytical testing.

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How do you handle discrepancies in analytical results?

Provide a clear method for addressing discrepancies, such as verifying tests, consulting with team members, and the steps you take to investigate and resolve these issues effectively.

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What strategies do you use to stay updated on advancements in chemistry and biochemistry?

Mention specific resources such as journals, webinars, or conferences that you use to keep your knowledge up-to-date, demonstrating your commitment to continuous learning and development in the field.

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Can you explain how you analyze and interpret analytical data?

Detail your approach to data analysis, including any software or methodologies that you use, focusing on how you derive conclusions that inform formulation and development decisions at Pace Life Sciences.

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Describe how you integrate teamwork into your Quality Control processes.

Explain features of your teamwork approach, particularly how you communicate with cross-functional teams, collaborate on projects, and ensure that all members are aligned towards common goals.

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How do you prioritize multiple projects in a fast-paced Quality Control setting?

Share your techniques for managing time and prioritization, such as task organization, setting deadlines, and effective communication with your team to ensure all projects stay on track.

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What is your familiarity with regulatory compliance in the pharmaceutical industry?

Discuss your understanding of relevant regulations, past experiences in ensuring compliance, and how you apply this knowledge to uphold quality standards in your work.

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At Pace®, we’re committed to continuously moving science forward to make an impact on the health and safety of our communities and lives. For decades, Pace® People have been committed to advancing the science of businesses, industries, consulting ...

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DATE POSTED
April 12, 2025

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