Quality Control Analyst

Posted 5 Hours Ago
Be an Early Applicant
São Paulo, BRA
In-Office
Mid level
Biotech
The Role
Perform QC batch release testing in chemistry and microbiology using HPLC, GC and microbial assays. Maintain cGMP documentation, support equipment calibration, investigations, CAPA/change control, method validation, author protocols/reports, train staff, and represent QC in audits and inspections.
Summary Generated by Built In

About This Role:
As a Quality Control Analyst, you will be a vital member of the Quality Control Lab, contributing to both the independent execution of laboratory activities and collaborative strategic projects. In this mid-level role, your expertise will span across QC Chemistry and Microbiology areas, where you will perform batch release testing and associated activities such as assay & impurities, pH, moisture, and chromatographic analyses. You will be responsible for ensuring robust and compliant cGMP documentation practices, maintaining data integrity, and adhering to GMP requirements to uphold quality standards. Your role will involve supporting equipment and instrument calibration programs, participating in key initiatives with external teams, and providing guidance to team activities as directed by management. Your collaboration will extend to investigations and compliance assessments, utilizing quality tools for managing deviations and corrective actions. Additionally, you will support method validation, author protocols and reports, and contribute to training programs. This position requires a good understanding of Health Authorities' regulations, representing QC in audits and inspections, and the ability to work effectively across all business areas and levels of the organization.

What You’ll Do:

  • Perform batch release testing in QC Chemistry and Microbiology areas.

  • Conduct chromatographic analyses including HPLC and Gas Chromatography.

  • Execute microbiological routine tests and microbial limits testing.

  • Maintain robust and compliant cGMP documentation practices.

  • Support equipment and instrument calibration program.

  • Participate in strategic projects and external team initiatives.

  • Collaborate in investigations and implement corrective actions.

  • Manage deviations, CAPA, Change Control, and other quality tools.

  • Support method validation and author protocols and reports.

  • Assist and contribute to training programs for employees.

  • Represent QC in audits and inspections with Health Authorities.

Who You Are:
You thrive in an environment where you can work independently yet enjoy collaborating with your team to achieve strategic goals. Your attention to detail and commitment to compliance are evident in your robust documentation practices. You are proactive in identifying areas for improvement and skilled in implementing corrective actions. Your excellent communication skills in both Portuguese and English enable you to effectively represent QC in audits and inspections. You are adaptable and capable of working across all levels of the organization, contributing positively to the team's success.

Required Skills:

  • 3+ years of relevant experience in Quality Control.

  • Bachelor’s degree in Pharmaceuticals or related Science fields.

  • Excellent written and verbal communication skills in Portuguese and English (advanced level).

Preferred Skills:

  • Master's degree or higher.


 

Job Level: Professional
Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.


At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about Biogen.


All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.



Skills Required

  • 3+ years of relevant experience in Quality Control
  • Bachelor's degree in Pharmaceuticals or related Science field
  • Excellent written and verbal communication skills in Portuguese and English (advanced level)
  • Good understanding of Health Authorities' regulations
  • Experience performing HPLC and Gas Chromatography analyses
  • Experience with microbiological routine tests and microbial limits testing
  • Experience maintaining cGMP-compliant documentation and data integrity
  • Master's degree or higher

Biogen Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Biogen and has not been reviewed or approved by Biogen.

  • Fair & Transparent Compensation Pay is generally positioned as competitive and often perceived as fair across roles, with total compensation framed as strong when bonus and equity are included. Compensation sentiment is described as above-average overall, though it varies by function and business cycle.
  • Equity Value & Accessibility Equity programs are repeatedly highlighted as a meaningful part of the total package, including stock programs and an employee stock purchase plan. Equity and bonus elements are portrayed as important contributors to feeling well rewarded beyond base pay.
  • Leave & Time Off Breadth Time-off benefits are described as distinctive, including a year-end shutdown and a paid sabbatical after extended tenure. Vacation, holidays, sick time, and personal-significance days are also presented as supportive of work-life needs.

Biogen Insights

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The Company
HQ: Cambridge, MA
9,575 Employees
Year Founded: 1978

What We Do

Through cutting-edge science and medicine, Biogen discovers, develops and delivers innovative therapies worldwide for people living with serious neurological and neurodegenerative diseases. Founded in 1978, Biogen is a pioneer in biotechnology and today the Company has the leading portfolio of medicines to treat multiple sclerosis, has introduced the first and only approved treatment for spinal muscular atrophy, and is at the forefront of neurology research for conditions including Alzheimer’s disease, Parkinson’s disease and amyotrophic lateral sclerosis. Biogen also manufactures and commercializes biosimilars of advanced biologics. With approximately 7000 people worldwide, we are truly a global organization, headquartered in Cambridge, Massachusetts, which is also home to our research operations. Our international headquarters are based in Zug, Switzerland and we have world-class manufacturing facilities in North Carolina and Denmark. We offer therapies globally through direct affiliate presence in 30 countries and a network of distribution partners in over 50 additional countries. For more information, please visit www.biogen.com. Follow us on social media – Twitter, LinkedIn, Facebook, YouTube.

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