Careers

Synthetic Chemist

We are currently looking for a dynamic and independent Synthetic Chemist . This position requires strong interpersonal and communication skills, leadership and teamwork.

As a MSc or PhD you must have at least 5+ years hands-on laboratory experience in synthetic chemistry within an industrial environment. The candidate must possess excellent synthetic organic chemistry skills.  Must have a proven track record of successfully managing teams of scientists on challenging projects with tight deadlines and demonstrate excellent supervisory capabilities. Candidates with experience in synthesizing libraries of small molecules will be given preference. Must have excellent communication skills both verbal and written and must be proficient at generating written technical reports

GMP Manuafcturing Manager

We are currently looking to add a Manager for our growing GMP API and Drug Product manufacturing division. An innovative leader with drive is required to bring the medicines of the future into clinical trials and commercial production. Responsibilities include planning and supervising the production of innovative pharmaceuticals in a GMP manufacturing setting in compliance with International Regulatory Requirements. The role requires strong Project Management skills and the coordination of equipment, materials, manpower and documentation. The management and leadership of a team of dedicated professionals and relevant departments are required to ensure delivery for clinical trials in order to meet client driven timelines and requirements. Responsible for production operations associated with the manufacture of all GMP products, you will develop weekly/monthly objectives as well as schedules, managing activities through line supervisors. You thrive on complexity and will also be responsible for trouble shooting and optimizing the scale up of batch production in a fast paced environment. With a science degree, in chemistry or Microbiology, you have at least 4 years experience in research and development as well as scale up in a pharmaceutical or biotech GMP manufacturing facility. A self motivated supervisor for a minimum of 3 years, you pride yourself on your ability to hire, motivate and develop high performing teams . The ability to communicate effectively both orally and in writing comes naturally to you; You are organized and have the ability to multi task effectively. Thorough knowledge and understanding of cGMPs and familiarity with FDA guidelines is required.

Formulation Specialist

Dalton is an international supplier of Pharmaceutical Services and Products. With the addition of solid dosage capabilities and an increased volume of business in our GMP Division, we are seeking a dynamic individual to add to our product development and manufacturing team. We are looking for a Formulation Specialist to be responsible for the formulation and development of liquid, solid and semi-solid drug dosage forms for novel molecules in clinical development. Duties include a hands-on role in making the greatest contribution to developing biologically and commercially appropriate formulations. Excellent communication skills and a professional manner are a must to ensure progress and timelines are shared with internal and external stakeholders. Working closely with the Analytical Chemistry section, the successful applicant will ensure required pre-formulation and compatibility testing is carried out to assist in the design, optimization and manufacture of innovative and biologically effective pharmaceutical formulations. A life long learner, you maintain an awareness of the latest scientific developments within the industry and recommend appropriate action where necessary. Beginning with the end in mind, you plan and co-ordinate the formulation and manufacture of appropriate product batches for product development, stability testing, pre-clinical testing, clinical testing and scale up from development to pilot scale. QUALIFICATIONS: BSc. or MSc. in Pharmaceutical Sciences, Chemistry or related field. The ideal candidate will have a minimum of 5 years of pharmaceutical industry formulation development experience with specific knowledge and capability in the area of dosage form development. Modified release formulation development experience is a definite asset Candidate must have a good understanding of the drug development process especially familiar with CMC and formulation related issues Demonstrated ability to work independently as well as a member of a team. Excellent oral and written communication skills Ability to prioritize work, adapt to change and complete projects on time and budget Thorough knowledge and understanding of cGMPs and familiarity with FDA guidelines is required.

Analytical Chemist

As an Analytical Chemist with a MSc in chemistry and 7+ years experience using HPLC and GC in the pharmaceutical industry, you are logical and have excellent oral and written communication skills.  You have great accuracy and precision in all testing that you conduct and interpretation of analytical data and technical report writing are your forté.

You will be required to conduct testing using a wide variety of equipment including HPLCs with UV, DAD, ELSD and electrochemical detectors, GCs (including capillary column and headspace) with FID and TCD detectors, Karl-Fischer, UV-vis, FTIR, oxygen headspace, Osmometer, automatic titrators, oxygen analyzers, pH meters, and also carry out wet chemistry analysis.  Your participation in development and validation programs will be required.

API Chemist

We are seeking a skilled Chemist with 2-3+ years pharmaceutical experience in manufacturing Active Pharmaceutical Ingredients. You have a BSc in chemistry, College Diploma or equivalent with Bench-scale laboratory skills and experience in synthetic organic chemistry.You are familiar cGMP guidelines. You will be involved in the set up, operation and cleaning of our production equipment and suites. You will manufacture chemical products according to the highest standards of quality and safety. You must be willing to work under a 7/24 schedule when required.

Sterile Fill Operator

Our Sterile Fill Team develops new processes to make sterile injectable products, primarily for clinical trials. The products include true solutions and suspensions including liposomal formulations. We are seeking a skilled individual to join our Sterile Fill Team. Qualified candidates will have a degree or diploma in Microbiology with 1-3 years of related work experience or a High School Diploma with 5+ years of related work experience and excellent verbal and written communication skills. You have experience in sterile products, specifically formulation and fill operations for small volume parenterals. You have an understanding of equipment configuration and work flow requirements for sterile filling operations. You have a good benchmarking knowledge of standard industry practices. You have experience with setup and operation of several types of filling lines. Your work experience will allow you to become sterile gowning qualified, participate in the sterile liquid formulation/filtration and fill of vials and or syringes. Experience in sterile powder filling is an asset. As part of the team you will share in the cleaning and set-up of our cleanroom suites and equipment. Your knowledge of cGMP guidelines and industry practices will also allow you to participate in project development and process validation, to ensure new products meet the highest standards of quality and safety. Willingness to work under a 24/7 schedule, when required, is a must