Mgr/Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have

Syneos Health Careers$100K — $130K *
US-AnywhereRemote in Canada
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 5-7 years of experience in regulatory affairs, particularly with CMC submissions
  • Deep knowledge of regulatory guidelines including FDA, EMA, and ICH
  • Bachelor's degree in a life-science field, preferably Biology, Chemistry, or Pharmacy
  • Strong interpersonal, strategic thinking, and problem-solving skills
  • Proficiency in handling compliance topics like change controls and GMP investigations

Responsibilities

  • Review CMC sections of regulatory submissions and agency interactions.
  • Develop global regulatory CMC strategies for commercial products.
  • Collaborate with regulatory teams on submissions and strategies.
  • Provide regulatory CMC guidance to cross-functional teams.
  • Support compliance assessments and manage deviations and investigations.

Benefits

  • Opportunities for professional development and growth
  • Collaborative and inclusive work environment
  • Engagement with cross-functional teams to enhance skills
  • Chance to work on impactful projects in regulatory affairs
Full Job Description
Mgr/Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have

Job Responsibilities

General Position Summary

The Chemistry Manufacturing Controls Manager will support the execution of global regulatory CMC strategies for marketed and development products. This role contributes to the preparation and submission of regulatory CMC documentation for a small molecule. This role also provides regulatory support and guidance to various cross functional teams to ensure all applicable global regulatory requirements are considered and appropriately incorporated into development and commercial programs.

Key Duties & Responsibilities
  • Reviews CMC sections of regulatory submissions, as well as the interactions and responses with regulatory agencies
  • Contributes to the development of global regulatory CMC strategies for commercial products
  • Works with regulatory colleagues in development of global regulatory CMC strategies and Submissions
  • Provides regulatory CMC guidance to cross-functional teams and key stakeholders
  • Supports regulatory assessment and guidance on product compliance topics including change controls, deviations, and GMP investigations

Required Education Level & Experience
  • Strong interpersonal skills to exchange complex information with others and to guide others
  • Proficiency in regulatory (FDA, EMA, Health Canada, LATAM, Middle East, and ICH) guidelines


  • Experience in the preparation, including writing, of CMC submissions
  • Strategic thinking and strong problem solving skills
  • Ability to collaborate and communicate in an open, clear, complete, timely and consistent manner
  • Strong sense of planning and prioritization, and the ability to work with all levels of management
  • Capable of strategic thinking with ability to resolve complex and ambiguous situations
  • Sound knowledge of cGMP, FDA, EMA, ICH
  • Bachelor's degree, with a preference in Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics or Medical Devices, or another related life-science field


Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms.

About Syneos Health Careers

Syneos Health Careers

Joining Syneos Health presents an unparalleled opportunity to become part of a global team of professionals dedicated to biopharmaceutical solutions. At Syneos Health, job opportunities abound, offering a gateway to enhancing career paths in a company celebrated for its commitment to therapeutic and operational excellence.

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Syneos Health is at the forefront of healthcare innovation, collaborating on projects that integrate smart technology and human ingenuity to improve patient outcomes. This dynamic company is actively seeking professionals who are eager to drive progress in the biopharmaceutical field through diverse job opportunities ranging from scientific roles to operational positions.

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For those starting their career, Syneos Health provides robust internship programs designed to foster professional growth and build essential industry skills. Interns at Syneos Health gain hands-on experience, beneficial for future employment opportunities within the company or the broader healthcare industry.

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Syneos Health is committed to the professional development of its employees, offering leadership training and career growth opportunities that encourage innovation and leadership skills. Employees are supported through comprehensive benefits, diversity training, and initiatives that promote personal and professional growth.

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