Skip to main content
Post your resume and find your next job on Indeed!

Pharmaceutical Engineering jobs

Sort by: -
    • Medical Devices (Class I–II).
    • Natural Health Products (NHPs/NPNs).
    • The RAS plans, authors, files and maintains regulatory submissions and dossiers, and ensures…
    • Lead code reviews, mentor junior developers, and enforce engineering best practices.
    • We manufacture our own line of advanced automation products for use in…
    • Experience in pharmaceutical manufacturing is preferred.
    • 1-3 years of experience in cGMP regulated pharmaceutical manufacturing environment.
    • Stay updated on industry trends, regulatory changes, and new technologies in the pharmaceutical field.
    • 2-5 years of relevant experience in in GMP QC laboratory…
    • Bachelor’s degree in engineering, construction or relevant field.
    • The role will support project delivery by attending meetings, taking minutes, and tracking…
    • Establish data engineering standards, best practices, and governance frameworks across the organization.
    • Establish talent development programs, technical career…
    • Proficient in interpreting engineering drawings and P&IDs.
    • Minimum of 3+ years of design engineering experience required.
    • Proficiency in SolidWorks and AutoCAD.
    • The successful candidate will have a minimum of 10+ years in a similar engineering and design role, with long-term team management experience to help manage,…
    • 5 + years of experience with process, mechanical design and/or manufacturing engineering experience, preferably in the pharmaceutical industry.
    • Support production and engineering teams while following all safety requirements.
    • At least 3 years of experience in a food, food ingredient, beverage or liquids…
  • View similar jobs with this employer
    • This role is responsible for actively identifying and qualifying prospective customers throughout Canada and Northeastern USA through the development of…
    • We are seeking a Project Manager / Regulatory Scientist to work in a multidisciplinary project environment to plan, supervise and manage projects and to…
    • Prepare engineering 3D models drawings of products and prototypes.
    • Graduated with a bachelor’s degree in engineering, Physical Sciences or an equivalent.
    • World Class Supplemental Health/Dental plans.
    • The Environmental Health & Safety Manager is responsible for promoting continuous improvement by the full…
    • Understanding of the pharmaceutical development sector considered an asset.
    • Bachelor’s degree in engineering, construction or relevant field.
Get e-mail updates for the latest Pharmaceutical Engineering jobs

By creating a job alert, you agree to our Terms . You can change your consent settings at any time by unsubscribing or as detailed in our terms.

People also searched:

engineer
engineer in training
engineering intern
engineering student
full time
mechanical engineer
mechanical engineering
part time
pharmaceutical companies
pharmacy

Career Resources:

Job Post Details

Pharmaceutical Regulatory Affairs Specialist - job post

CRL Synergy
Calgary, AB T2S 1W3
$68,000–$100,000 a year - Full-time

Job details

Pay

  • $68,000–$100,000 a year

Job type

  • Full-time

Location

Calgary, AB T2S 1W3

Benefits

Pulled from the full job description

  • Paid time off
  • Vision care
  • Dental care
  • Life insurance
  • Disability insurance
  • On-site gym
  • Extended health care

Full job description

Job Overview
CRL Synergy, one of Canada’s largest and fastest-growing suppliers of control label products, is seeking a detail-oriented and proactive Regulatory Affairs (RAS) Specialist.CRL Synergy is seeking a Regulatory Affairs (RAS) Specialist who can thrive in a fast-paced environment that involves working in an office team environment.

The Regulatory Affairs Specialist is the site lead for all Health Canada submissions and post-market activities covering four product categories sold across Canada:

  • Drugs (DIN-assigned OTC)
  • Cosmetics
  • Medical Devices (Class I–II)
  • Natural Health Products (NHPs/NPNs)

The RAS plans, authors, files and maintains regulatory submissions and dossiers, and ensures compliant labelling/advertising.

This role will also provide quality assurance support through maintenance of the RA SOPs, ensuring they are current and implemented, perform data collection, and subsequent analysis.

The successful candidate will provide support for new product development, ensuring Health Canada and customer requirements are being met, including labelling accuracy for new and modified product.

Responsibilities

  • Oversight of Pharmacovigilance program

· Collaborate with cross-functional teams to implement corrective and preventive actions (CAPA) related to customer complaints.

· Participate in risk management activities and contribute to the development of risk assessment strategies.

  • Ensuring accurate record keeping and filing as per organizational procedures.
  • Handle clerical and administrative activities.
  • Review and assess customer complaints for adverse reactions and reportable incidents. Perform surveillance activities for ongoing product quality and safety.
  • Complete Annual Summary Reports and perform screening of scientific literature for product safety information.
  • Assisting in updating methods and procedures (SOPs) related to the Quality Management System with a focus on the customer complaint and pharmacovigilance program.

Qualifications

  • Bachelor’s degree in a relevant field; advanced degree preferred.
  • Proven experience in regulatory affairs or a related field, with a strong understanding of compliance requirements.
  • Demonstrated skills in project management, including the ability to manage multiple projects simultaneously.
  • Strong leadership abilities with experience in supervising teams or mentoring staff.
  • Excellent analytical skills with a focus on process improvement methodologies.
  • Familiarity with sales or business development processes is a plus.
  • Exceptional communication skills, both written and verbal, with the ability to effectively convey complex information to diverse audiences. Join us in making a difference through compliance excellence!

Job Type: Full-time

Pay: $68,000.00-$100,000.00 per year

Benefits:

  • Company events
  • Dental care
  • Disability insurance
  • Extended health care
  • Life insurance
  • On-site gym
  • On-site parking
  • Paid time off
  • Vision care

Education:

  • Bachelor's Degree (preferred)

Experience:

  • Regulatory Affairs: 2 years (preferred)

Work Location: In person

Let Employers Find YouUpload Your Resume