Careers

Theratechnologies is continually seeking talented, energetic people that share our values. If you want to join an exceptional team in a dynamic and respectful work environment with exciting new challenges that motivate people to excel and go above and beyond for healthcare professionals and patients, we invite you to submit your resume.

Even if there is no currently available position that corresponds to your experience, we invite you to submit your resume for future opportunities.

Embracing Diversity and Inclusion

Theratechnologies understands and values the uniqueness of each individual and recognizes the importance of diversity in the workplace. Our team members originate from all over the world: Asia, Europe, South America, North America, the Caribbean and the Middle East. We nurture an empowering environment to make each individual feel safe, appreciated and respected.

The ethnocultural, racial and age diversity within Theratechnologies makes our teams stronger and brings innovative ideas and new perspectives to the table. Therefore, we are committed to providing our employees with equitable treatment and respecting the unique nature of each individual, experience and tradition; and this is achieved by:

 

 

Establishing a sense of belonging for our employees

 

Ensuring that every person is heard and respected

 

Maintaining a supportive leadership style to help each team member thrive

Careers

Job Opportunities

Send your application to cv@theratech.com

Position Summary

The incumbent provides support to the regulatory team with all submissions filed to the health authorities aligned with the global regulatory strategies in support of these filings for new and approved products; assists with information requests for dossiers under active review; and ensures that marketing authorizations for company products are maintained as per applicable Federal Regulations and Guidance in various jurisdictions and throughout the product(s) lifecycle.  We are seeking a talented and experienced regulatory affairs subject matter expert who is excited to join a dynamic and growing organization and who is committed to deliver excellence in all projects under their responsibility.

Key Responsibilities

  • Support all regulatory activities related to company product(s)
    • Manages regulatory activities to obtain and maintain Marketing Authorizations from FDA, Health Canada, EMA and other health authority regulations as applicable for commercial products. 
    • Assists with the compilation, authoring, review and submission of dossiers to regulatory authorities and ensures documents meet applicable regulatory requirements.
    • Provides regulatory input to the development and implementation strategy for new products/projects. 
    • Assists to provide regulatory guidance regarding the documentation needed and requirements for regulatory submissions per applicable guidelines.
    • Assists to provide regulatory support and expertise for early phase clinical trials; and pre-IND/clinical development/scientific advice meetings with regulatory Agencies; and the filing of IND/NDA/BLA and related submissions to FDA, EMA, Health Canada and other health authorities as applicable.
    • Assists with/ coordinates the preparation of responses to information requests from health authorities; and subsequent follow-ups with regulatory agencies to maintain and update existing marketing authorizations.
    • Facilitates approval of new product licenses, indications and dosage strengths.
    • Supports regulatory activities relating to product launches; maintains compliance of existing assigned product licenses with applicable health authority regulations.
    • Participates and supports Global RA for applications filed under the EU systems, namely Mutual Recognition and Centralised procedures.
    • Maintains local RA databases and global compliance tracking systems to record license information (new indications, changes in indications, changes in product specifications, changes in licensing, new products and progress with development of new products).
    • Provides support to various partners, CROs and US/EU Agents to support registration of Theratechnologies’ product(s) and Market Authorizations in other territories/ countries; and liaises with the respective Health Authorities as needed.
    • For commercial products, reviews and approves proposed change controls from a regulatory perspective as per FDA, Health Canada and EMA regulations and guidance. 
    • Assists with the coordination of Product Recall activities and necessary regulatory actions.
    • Provides regulatory support and guidance to internal and external customers.
    • Analyzes product information, compiles and communicates annual notifications to Health Canada.
    • Maintains current knowledge of relevant ICH, FDA, Health Canada, EMA and other health authority regulations as applicable.
    • Ensures that regulatory guidance documents and regulations, as well as internal procedures are followed in order to maintain regulatory compliance.
    • Fosters good relations with the respective Health Authorities.
       
  • Execution of regulatory dossier preparation, reviews and audits
    • Reviews and updates product labels, product monographs and labelling / packaging artwork.
    • Prepares and reviews INDs, NDAs, BLAs, PSURs/PADERs, Annual Reports, and updates to Investigational Brochures to Regulatory agencies.
    • Assists with the preparation of DEL amendments, Annual Licence Renewals, Notifiable Changes, and PMPRB forms for submission to Health Canada.
    • Assists with the preparation of post-approval variations, extensions and renewal of MAA/ market authorizations with EMA.
    • Assists the team with health authority inspections, internal and external audits according to the approved audit plan/schedule, and with supplier audits as necessary.
    • Reviews reports and other regulatory documentation from Contractual Research Organisations (CROs). 
       
  • Point of contact for regulatory documentation
    • Provides support to internal departments to ensure regulatory compliance with regulations in respect of company products. 
    • Produces, reviews and submits various documents/reports related to regulatory submission requirements.
    • Assists with the writing of Standard Operating Procedures (SOPs) pertaining to the regulatory function and revisions thereof and ensures their adherence.
       
  • Performs any other related tasks as assigned by management

External Customers

  • Health Canada, US FDA, European Medicines Agency (EMA) and other government regulatory agencies 
  • US, Canada and EU Regulatory Agents and Contractual Research Organisation (CROs)
  • External Consultants

Required Qualifications

  • B.Sc./ Life Sciences University degree in a scientific field or equivalent, or other scientific background that is deemed appropriate 
  • Minimum 5 years of experience in regulatory affairs in pharmaceutical drugs and /or biologics in the pharma industry 
  • Regulatory experience in medical device industry is an asset
  • Excellent knowledge and comprehension of Canadian and US Regulations; good knowledge of European regulations is an asset
  • Regulatory affairs experience in HIV and Oncology is an asset, or other therapeutic areas 
  • Good understanding of preclinical and clinical research is an asset
  • Prior experience in regulatory audits is an asset 
  • Experience of managing external partners/CROs is an asset
  • Experience with eCTD publishing is an asset   
  • Good knowledge of Word, Excel, Power Point and Outlook
  • Ability to conduct Internet searches in respect of regulatory matters 
  • Demonstrated skill in managing multiple projects/priorities
  • Effective communication and negotiation skills
  • Bilingual in French and English, oral and written 

Personal Qualities for all Personnel

  • Ability to set goals and meet deadlines
  • Ability to prioritize
  • Ability to generate ideas and find solutions
  • Ability to work independently
  • Able to work well in a team environment and communicate well
  • Versatility and flexibility

Personal Qualities Specific to the Position

  • Interpersonal ability and diplomacy  
  • Attention to detail and quality
  • Good stress management
  • Ability to influence others 
  • Multi-tasking
  • Interpersonal leadership
  • Planning and organizational skills
  • Available for occasional business travel

Position Summary

The incumbent supports the Associate Director, Global Quality Assurance (QA) in order to ensure the consistency of the quality standards as per the Good Manufacturing Practices (GMP) during the documentation review, including but not limited to the specifications, master documents, change control, complaints, audits, CAPAs, SOPs, etc; to approve or reject the release of Active Pharmaceutical Ingredients (APIs),finished drug product batches, and /or injection kits.  We are seeking a talented and experienced quality assurance subject matter expert who is excited to join a dynamic and growing organization and who is committed to deliver excellence in all projects under their responsibility.

Key Responsibilities

  • Support in the QA activities
    • Reviews specifications and acceptance criteria
    • Ensures that the products’ manufacturing, packaging and testing are defined, controlled and in conformity with GMPs
    • Reviews stability data and approves retest or expiry date
    • Evaluates the APIs and end-products’ quality and determines whether to withhold the batches or release them
    • Ensures that all manufacturing steps are followed and in conformity with GMPs
    • Participates in complaints’ evaluation in order to identify the causes and recommends corrective/preventive actions.
    • Evaluates incidents and provides corrective/preventive actions
    • Participates /supports regulatory audits
    • Reviews/evaluates change controls
    • Ensure timely completion of deviations, complaints, CAPAs, change controls, etc. as per established procedures
    • Contributes to the maintenance of the Quality System and the KPIs report
    • Escalates any deviation to GMPs, complaints or risk assessments that may impact the patients’ security or the product’s quality, integrity or purity
       
  • Support in the compliance-related activities
    • Ensures that policies and procedures are written and revised to ensure their conformity with regulatory standards
    • Reviews all documents, packaging and labels to ensure conformity
    • Participates in the preparation and presentation of the Annual GMP training
    • Supports regulatory audits
       
  • Key resource person for Quality Assurance matters
    • Acts as the representative of the quality team in the various committees and working groups
    • Evaluates and ensures the disposition of returned product
       
  • Documentation, procedures and systems 
    • Reviews/approves masters, including specifications, manufacturing and packaging master batch records, protocols, validation reports and any other GMP documents
    • Verifies temperature data during the transportation of the products and determines their status/disposition
    • Determines the disposition of a nonconforming product and proposes the necessary solutions
    • Evaluates/approves change controls, audits, out of specifications  investigations and external suppliers’ deviations
    • Reviews the manufacturing documentation and the investigations for customers’ complaints related to product manufacturing and packaging
    • Drafts and/or approves external procedures, specifications, risk assessments, deviations, preventive/corrective measures, change controls, etc.
    • Prepares forms, memos, lists and reports as required.
       
  • Performs any other task as requested by management

External Customers

  • Contracted Partners
  • Suppliers

Required Qualifications

  • Bachelor’s degree in Pharmacy, Chemistry, Biology or Chemical Engineering
  • Training in Quality assurance
  • 5-8 years of quality assurance experience in the pharmaceutical industry, ideally with sterile products, pharmaceutical a/o biological products
  • Good understanding or experience in laboratory research, pre-clinical and/or clinical research is an asset
  • Experience with regulatory inspections, supplier audits and internal audits
  • Experience in policies and procedures related to the pharmaceutical compliance program
  • Excellent knowledge of the GMP, GLP, GDP, as well as the pharmaceutical industry’s guidelines and regulations in Canada and United States
  • Knowledge of the pharmaceutical industry guidelines and regulations in Europe is an asset
  • Knowledge in Good Clinical Practice is an asset
  • Knowledge of Word, Excel, PowerPoint and Outlook
  • Previous experience working with databases
  • Bilingual French and English, spoken and written
  • Excellent English authoring/writing skills 

Personal Qualities for all Personnel

  • Ability to define objectives and meet timelines
  • Ability to determine priorities
  • Ability to bring ideas and find solutions 
  • Can work alone or in a team
  • Team spirit and collaborative
  • Flexibility

Personal Qualities Specific to the Position

  • Leadership and accountability
  • Result-oriented
  • Ability to negotiate and influence others
  • Multitasking
  • Analytical capabilities and ability to synthesize information
  • Planning and organizational skills
  • Good stress management
  • Attention to detail and quality
  • Verbal and written proficiency
  • Thoroughness in accomplishing tasks
  • Available for occasional business travels

Position Summary

Responsible for the organization and co-ordination of office operations, procedures, and resources to facilitate organizational effectiveness and efficiency.

This position is based in Montreal, Quebec

Key Responsibilities

  • Responsible of our office operations, including facilities management, inventory management (supplies, food, and beverages, etc.), vendor management, reception, etc. 
  • Be the go-to person for office supply ordering, catering, and overflow in supporting the executive assistants
  • Provide general facilities support including initiatives related to hybrid work environments, office space, and local requirements.

Administrative Office Coordinator and Receptionist tasks (70%)

  • Manage general office needs including ordering office supplies and weekly food orders, maintaining a stocked kitchen 
  • Create an office supplies inventory to ensure a proper upkeeping of re-stock orders
  • Source supply vendors and maintain vendor agreements and act as their primary contact. 
  • Respond to facility issues and coordinate with the building property management, including all requests/issues related to the work environment, including the office kitchens (i.e., temperature in the offices, office and kitchen equipment repair and maintenance ex.: dishwasher, water coolers...etc...). 
  • Organize and distribute office supplies (stationery and kitchen) equally amongst both floors
  • Ensure conference rooms are prepared for meetings.  
  • Maintain the reception area, keeping it clean and free of clutter. 
  • Organize deliveries and mail and ensure distribution to the correct recipients in a timely manner; manage the office mailbox and any outgoing mail and packages for pickup.
  • Assist HR and IT with onboarding and offboarding tasks; Coordinate all key, security card, and maintenance requests as required 
  • Coordinate and assist with office event planning
  • Create a safe work environment for all employees and visitors

Support to the Executive Assistant (30%)

  • Support in organizing meeting rooms, before and after the meetings.
  • May be requested to provide clerical, administrative, and secretarial responsibilities 
  • May be called to help organize  appointments and meetings
  • Other duties, as assigned.

Job Qualifications and Requirements

  • CEGEP diploma or equivalent, or High school diploma combined to 1-2 years of experience in administrative and procurement-related 
  • Proven work experience as a Receptionist, Front Office Representative, or similar role.
  • Proficient with MS Office 
  • Bilingual, verbal and written
  • Resourceful and proactive when issues arise
  • Excellent organizational, multitasking and time-management skills, with the ability to prioritize tasks.
  • Customer service attitude, social, ability to interact with multiple people.
  • Integrity, teamwork, and collaboration

External Customers

  • Contracted Partners
  • Suppliers

Job Description

The Medical Advisor is responsible for the scientific integrity of the clinical development program and the translation of scientific information for tesamorelin into business concepts. The Medical Advisor will support the medical community and develop advocacy for the product. The Medical Advisor will also support the elaboration of abstracts and manuscripts for publication.

Key Responsibilities

  • Responsibilities of the Medical Advisor Endocrinology are covering different therapeutic areas (including NASH and HIV) and also different life cycle management
  • Provides deep medical/scientific expertise and medical affairs leadership and supports various functional areas.
  • Provides expert product and therapeutic area medical expertise, as well as relevant scientific information in response to customer-stated needs.
  • Develops customer advocacy to support brand business objectives and gathers insights to inform future brand strategies.
  • Contributes to the brand strategy and develops a medical strategy to be executed as defined.
  • Elaborates scientific rationale for medical and commercial projects and review new clinical study protocols and investigator-initiated research proposals.
  • Participated to abstracts and manuscripts writing for publication.
  • Manage clinical study(ies) and medical project(s).
  • Supports the development of symposia and continuing medical education initiatives.
  • Support clinical study feasibility, site mapping, identification and participation and provide support with resolving any pending issues with the study sites.
  • Collaborate with the project manager to manage clinical studies and write clinical study documentation.
  • Supports Regulatory Affairs and Pharmacovigilance department to establish program/product regulatory strategies that best support product medical and commercial objectives. Leads key cross-functional initiatives relating to Regulatory submissions.
  • Be an internal scientific resource and trained commercial and medical colleagues.

Job Qualifications and Requirements

  • Doctoral degree (MD, PharmD, PhD) in a medical/scientific discipline
  • At least 5 years in the pharmaceutical industry
  • Experience in clinical research is an important asset
  • Fluency in English, written and spoken, Spanish is an asset
  • Good oral presentations skills, writing skills and aptitude for creating reports
  • Autonomy and initiative
  • Good team communication skills and team spirit
  • Good planning and organizational skills
  • Good leadership skills.
  • Clinical trials/research experience a strong asset

Personal Qualities for all Staff

  • Ability to communicate scientific and clinical information clearly and credibly verbally and in writing
  • Interpersonal: ability to interact easily with all levels within the organization in a tactful, mature and flexible manner
  • Must act ethically and with integrity
  • High level of collaboration and influencing skills
  • Ability to work independently and within cross-functional teams
  • Excellent people leadership and organizational skills
  • Ability to make sound and compliance guided judgments
  • Must be a self-motivator with strong drive for result driven success
  • Versatility and flexibility.

Job Description

The incumbent will be responsible for establishing and managing all the supply chain related activities for the clinical projects at Theratechnologies Inc. Please note that this position may be based in Dublin, Ireland, or Montreal, Quebec, Canada, depending on the location of the successful candidate.

Required Qualifications

  • Bachelor's degree in science or equivalent
  • 5 years of team management experience
  • 5 years of relevant experience in a supply chain role
  • 5 years of experience in a pharmaceutical or biotechnology company
  • Good knowledge of European guidelines, laws, regulations, and regulatory practices (Good Manufacturing Practices (GMP), Good Distribution Practices (GDP))
  • Excellent communicator, and well-organized with superior presentation skills
  • Understand the quality mechanisms for releasing batches of manufactured drugs.
  • Knowledge of Word, Excel, Power Point, Outlook, and Project

Job Description

Under the supervision of the Manager, Chemistry, the Drug Discovery Scientist is responsible for managing a variety of activities, including the synthesis and purification of new anti-cancer molecules, and the development and validation of analytical methods. He/She will develop protocols and carries out experiments using medicinal chemistry and appropriate laboratory equipment; carry out tests on pharmaceutical substances, pharmaceutical products and stability samples in support of the development and manufacturing of drugs; collect and interpret analytical data and draft reports in conformity with the laboratory’s SOPs.

Required Qualifications

  • Education/Experience: Bachelor’s or Master’s degree in Chemistry or a related scientific field with 3 to 5 years of experience in analytical chemistry/development/method validation
  • Skills in synthesis or combination chemistry
  • Technical skills: Ability to use AKTA, HPLC, UPLC, LC-MC, UV-VIS spectrophotometer, PH meter, and other modern analytical equipment
  • Problem solving: Ability to solve technical problems and provide a timely and satisfactory resolution
  • Verbal communication: Communicate efficiently with other team members of various departments, and with clients in a clear and concise manner
  • Written communication: Complete documents and journals in a clear and exact manner; draft clear and precise technical documents
  • Experience in a pharmaceutical laboratory or an equivalent combination is required
  • Ability to draft reports and effectively present the information
  • Reasoning skills: Ability to determine problems, collect data, establish facts and draw valid conclusions; interpret, mathematically or in the form of a diagram, a big variety of technical instructions and process several abstract and concrete variables
  • Computer skills: To successfully undertake this work, a person should have basic computer skills with a knowledge of MS Suite products and the ability to effectively and securely use the Internet tools