Pharmacy Tech I

May 7 2024
Industries Pharmaceutical, Biotechnology
Categories Pharmacy
Quebec, QC • Full time

Description

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE

Why Syneos Health

  • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
  • We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
  • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong.

Job responsibilities

  • Carries out all activities related to receiving, handling, inventory, the dispensing and disposal of investigational products.
  • Participates in the review or the development of pharmacy manual, protocol, and other applicable documents.
  • Verifies all information or data sent by clients and ensures that the product received complies with the specific clinical study objectives and with laws and regulations.
  • Ensures that the product is kept under appropriate storage conditions.
  • Ensures that there is a sufficient inventory of supplies for study needs, and places orders for more supplies as needed.
  • Processes aseptic preparation (reconstitution/dilution) and nonsterile compounding.
  • Participates in the peer-review process for raw data and performs follow-up within the required timeframes.
  • Communicates with internal resource people for all details related to the pharmacy and identifies potential problems and communicates opportunities to improve and/or amend a procedure.
  • Participates in client visits, including sponsor or regulatory agency audits and participates to the project trusted process.
  • Updates the Trial Master File (TMF) as required.
  • Ensures that pharmacy equipment is well-maintained and in good condition and takes appropriate actions when required. Can be called upon to acknowledge an environmental monitoring alarm and apply corrective actions.
  • May be involved in training of employees for some pharmacy-related tasks.
  • May be assigned other clinical tasks.

Qualifications

What we're looking for

Position in Canada

  • The incumbent should possess a vocational diploma in health, pharmacy technical assistance program or College Degree in pharmaceutical product (A.E.C.).
  • English level: Required bilingualism includes understanding various messages, exchanging verbally on subjects related to the tasks to be executed, and writing messages/procedures.
  • Must demonstrate good computer skills especially in the utilization of Microsoft Word and Excel.
  • Demonstrate problem solving, strong organizational and interpersonal skills.
  • Experience in regulatory context will be considered an asset.
  • Experience in parenteral preparation.
  • Excellent communication, presentation, interpersonal skills, both written and spoken.
  • Experience in regulatory context will be considered an asset.
  • Candidate who does not possess the required training and/or experience may be considered under different criteria.

Position in US

  • The incumbent should possess a vocational diploma in health or pharmacy technical program.
  • Spanish level: N/A
  • Must demonstrate good computer skills especially in the utilization of Microsoft Word and Excel.
  • Demonstrate problem solving, strong organizational and interpersonal skills.
  • Experience in regulatory context will be considered an asset.
  • Experience in parenteral preparation.
  • Excellent communication, presentation, interpersonal skills, both written and spoken.
  • Experience in regulatory context will be considered an asset.
  • Candidate who does not possess the required training and/or experience may be considered under different criteria.


Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

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. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

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