Pinewood Healthcare is a leading developer, manufacturer and marketer of healthcare products, currently employing over 320 people across two sites in Tipperary and Dublin. Originally established in 1976 to serve the renal care market in Ireland, Pinewood evolved over the years under indigenous Irish ownership until its sale in 2006 to the Wockhardt Group, an Indian global pharmaceutical and biotechnology company headquartered in Mumbai, India. Wockhardt employs over 7,000 people across 27 nationalities with a presence in the USA, UK, Ireland, Switzerland, France, Mexico, Russia and many other countries. It has manufacturing and research facilities in India, the USA and UK and a manufacturing facility in Ireland (Pinewood Healthcare).
JOB RESPONSIBILTIES
1. Assist in the completion of formulation of new products to meet customer requirements.
2. Product evaluation, formulation development and sample preparation.
3. Maintaining samples and products development stock area.
4. Internal product technical support.
5. Employ skills in the design and data analyses of experimental studies.
6. Able to integrate experimental design expertise with technical knowledge.
7. Execute experimental work to meet project goals and timelines.
8. Manufacture, packing and evaluation of stability samples for development pharmaceutics.
9. Work to tight production planning and deadlines.
10. Assist compatibility studies and scale up processes.
11. Be aware of existing quality procedures.
12. Calibration of instruments and equipment in the laboratory.
13. Oversight of relevant development pilot batch manufacture in production.
14. Provide process transfer support for technical transfers.
15. Ensure that all work carried out is in compliance with the required standards conforming to company cGxP, SOPs, regulatory regulations and guidelines, safety and environmental guidelines.
16. Any other duties as deemed appropriate and as designated by the role holder's line manager.
SKILLS, QUALIFICATIONS AND EXPERIENCE
a) BSc in Science or Engineering or related discipline, post graduate qualification highly desirable..
b) 0-2 years' experience in a pharmaceutical R&D / testing environment is preferred.
c) Must possess a knowledge of oral drug product development.
d) Excellent analytical skills, oral and written communication skills, as well as a demonstrated ability to operate both independently and in team settings.
e) Must be willing to work on multiple projects.
f) Ability to be self-motivated and focus others with respect to implementing identified improvement initiatives.
g) Have demonstrated effective research skills, including the critical review of the scientific literature.
h) Excellent technical writing skills.
