Recruitment
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EirGen Pharma, based in Waterford, Ireland, is currently recruiting for quality control chemists, analytical development chemists, regulatory affairs officers, and QA officers. EirGen is the supply chain and R&D center of excellence for OPKO Health, exporting medicines to over 45 countries worldwide. The company employs over 170 people from 9 nationalities and offers a competitive benefits package.
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Warm Greetings from Chempro Pharma! Here is a brief presentation regarding our newest project/service offering - pharmaceutical product development. We have a highly specialized team that has worked with the likes of Novartis, Merck and many more market leaders within the pharmaceutical industry. Feel free to review this attachment and contact us at pharma@chemprogroup.net if you have any questions, thanks!
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This document describes the many services provided by LGC including:
- Supporting pharmaceutical research and ensuring safe drug development.
- Providing reference standards and testing for foods, supplements, chemicals and other products to ensure safety and quality.
- Offering forensic testing and expert services to help solve criminal cases.
- Facilitating research across many areas of science through the development of testing methods and reference materials.
Tbi Bioprocessing Services Sept 25.08
Therapure Biopharma provides bioprocessing services including technology transfer, process development, testing, validation, manufacturing, and project management. Located in Mississauga, Ontario, Therapure has expertise in developing and manufacturing proteins and biologics for clinical and commercial applications. Their services help clients bring products from pre-clinical through commercial stages while ensuring quality and regulatory compliance.
Marketing II: Indu Isaacs
The document describes the services of a contract development and manufacturing organization called Lowell and Andover. It outlines their capabilities in formulation development, analytical development, manufacturing, and regulatory experience assisting clients from discovery through post-approval. Their goal is meeting expectations for timelines and producing consistent, stable dosage forms to help clients advance products at the speed of science.
genpharma english
Genpharma aims to strengthen its global presence as a recognized manufacturer of quality finished drug formulations. It provides products on time and focuses on regulatory documentation, product delivery, and after-sales service. Genpharma emphasizes quality control and assurance at each stage of production according to good manufacturing practices and regulatory standards. It uses modern equipment and qualified staff for rigorous testing and analysis to achieve high product quality. Genpharma is developing manufacturing facilities in India, Malta, and Uzbekistan to produce finished dosage forms meeting international guidelines.
Astral Pharmaceuticals
Astralpharma - India's one of the leading Pharmaceutical Manufacturing Company. Contact premier distributor of Pharmaceutical
Manufacturing Company India from www.astralpharma.net.
ClinActis: Logistics of Asian Based Clinical Trials
ClinActis Overview:
ClinActis Pte Ltd is a full service CRO providing clinical trial services to the pharmaceutical, medical device, medical nutrition and biotech companies in Asia Pacific. Established in 2009, ClinActis Pte Ltd is headquartered in Singapore.
ClinActis Experience:
• 33 years experience in clinical research in pharmaceutical and biotechnology companies as well as CROs
• 27 years experience in Asia Pacific, including Australia/New Zealand, China, Malaysia, Hong Kong, India, Indonesia, The Philippines, Singapore, South Korea, Taiwan, Thailand and Japan
• Extensive knowledge of regulatory frameworks, best KOLs and sites across the region
• Vast therapeutic experience including Cardiovascular, CNS, Endocrinology, Infectious diseases, Oncology, and Respiratory
Piramal Clinical Trial Services
Piramal Clinical Trial Services provides clinical trial manufacturing capabilities including packaging, storage, distribution, and reconciliation of investigational drugs. They offer primary and secondary packaging, kit preparation and compilation, temperature controlled storage and distribution, returns management, and support services globally. Piramal aims to offer superior customer service and uses a digital platform called TrakPack to track manufacturing, distribution, returns, and provide reporting to customers.
LGM Pharma | Drug Research & Development APIs
LGM Pharma is a leading innovative U.S. supplier and distributor of active pharmaceutical ingredients (APIs) to pharmaceutical, manufacturing, biotech, and pharma R&D markets.
Karen Campbell Resume 2016
Karen Campbell is seeking a position that utilizes her experience in quality assurance and process improvement. She has over 30 years of experience in medical laboratories and 13 years as Quality Assurance Manager at ThermoFisher Scientific, where she developed quality processes, standard operating procedures, metric boards, and led corrective actions. She is trained in Lean Enterprise techniques and served as an internal ISO auditor.
CV Jess Mc Govern 15
Jess Mc Govern has 3 years of experience in a GMP laboratory, including method development, validation, equipment qualification, data review, and training. They hold a BSc in Industrial Biochemistry and are proficient in analytical techniques like HPLC, GC, and UV/Vis. In their current role at Eurofins Lancaster Laboratories, they perform pharmaceutical analysis, write reports, and assist in management responsibilities. They are organized, a strong communicator, and enjoy artistic pursuits and traditional Irish music in their free time.
Salim qc cv
Abdul Salim is applying for a position and has over 8 years of experience in quality control for food industries. He currently works as the Quality Control Incharge, Food Safety Team Leader, and Document Controller at a dairy and juice company in Qatar. His CV details his relevant work experience and education, including an M.Sc. in Applied Microbiology.
Resume N
This document contains the resume of Sudhanshu Tripathi, who has 6 years of experience as a Quality Executive in the food manufacturing industry. He has expertise in quality assurance, quality control, implementing food safety systems like HACCP and ISO 22000. He is seeking a role as a Quality Executive where he can oversee quality operations and ensure compliance with food safety standards. His professional experience includes roles at various food manufacturing companies where he was responsible for quality management, audits, supplier evaluation and ensuring product quality.
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Recruitment
- 1. EirGen Pharma, part of OPKO Health Inc., is based in Waterford in the South East of Ireland and are currently recruiting for a number of positions including: • Quality Control Chemists (ref: QC) • Analytical Development Chemists (ref:AD) • Regulatory Affairs Officer / Specialist (ref:RA) • QA Officers (ref:QA) EirGen Pharma is the Supply Chain and Research & Development Centre of Excellence for OPKO Health, exporting life-saving medicines to over 45 countries worldwide. Our current site is an Oral Solid Dose Facility and our 2nd site (opening later this year) is a state of the art Research & Development & Sterile Fill Finish Facility. We currently employ over 170 people, representing over 9 nationalities, and we offer competitive salary, health insurance, pension and additional holiday leave as part of our remuneration package. Our QC Chemists test all raw materials, packaging, finished product and stability samples using a broad range of analytical techniques in a GMP environment. Our Analytical Development Chemists develop, validate, troubleshoot and transfer analytical methods, draft scientific protocols and reports, and perform release testing of development batches, clinical batches and submission batches. Our Regulatory Affairs Officer / Specialists support the compilation of CTD dossier for global territories including EU and USA and our QA Officers develop, implement and maintain EirGen quality standards and systems to ensure that our products comply with Marketing Authorisations, documentation, specifications and cGMPs. Applicants must be qualified to degree level in pharmaceutical science, with at least 3 years previous pharmaceutical experience, preferably working in an English speaking environment. Applicants must also have excellent written and verbal English and will undertake skype screening interviews if shortlisted. To find out more about these exciting opportunities, check out www.eirgen.com for more information or email hr@eirgen.com to apply.