Scientific Search specializes in Pennsylvania Pharmaceutical Recruiting and staffing for a broad spectrum of technical and scientific positions within the Pharmaceutical, Biotechnology and Medical Device industries. We have a dedicated Pennsylvania Pharmaceutical Recruiting team that focuses exclusively on this segment. Positions include technical, management and executive levels (including Directors and Vice Presidents) and many segments such as discovery research, clinical research, regulatory affairs, medical education, quality control, engineering, operations and marketing. Call or email us today and let us show you what our Pennsylvania Pharmaceutical Recruiting team can do!
Some typical positions that we have placed are:
Brand Management
Chemist
Clinical Research
Compliance
Continuing Medical Education (CME)
Documentation Control
Drug Safety
Marketing
Medical Director
Laboratory
Medical Device Manufacturing
Medical Science Liaison (MSL)
Operations
Packaging
Product Development
Quality Assurance
Quality Control
Regulatory Affairs
Sales
Scientist
Technology Transfer
Validation
Our internal database contains thousands of qualified pharmaceutical, biotech and medical device professionals that our Pennsylvania Pharmaceutical Recruiting team has established relationships with. We are typically able to provide you with outstanding candidates within days of a request if not sooner. Here are some candidates our staff has identified as exceptional in what they do, and potentially high impact hires at their new organizations:
Featured Pharmaceutical Candidates
211,041 – Director, Global Medical Affairs – 20 years experience in industry, 11+ in management. PharmD with an MBA and has 12 years of medical affairs experience at a Biologics company at the Director level. Act as alliance management group lead across international partnerships for near-market and marketed products; implement terms for alliance governance and protocols for working together. Partner with Clinical, Commercial, and Compliance teams across organizations to ensure that goals and objectives are aligned, understood, and integrated. Communicate regularly with affiliate personnel to ensure harmonization and transparency of activities. For additional information on this exceptional candidate please contact Michelle Lair, michellel@scientificsearch.com.
194,938 – Director, Medical Affairs – Lead planning and execution of global advisory board meetings and life cycle management initiatives. Lead competitive intelligence planning and execution for cardiovascular franchise. Co-lead the development of a global scientific platform for product launch planning. Serve as US Medical Research Lead on post-marketing studies and Investigator Initiated Studies. Build product advocacy through relationships with Key Medical Leaders and medical congresses. Serve as scientific resource to Field Medical Affairs, Medical Information, Sales &Marketing, Advertising Review Committee, Health Economics Outcomes Research, and Global Brand Team. PharmD; BS – Microbiology. For additional information on this exceptional candidate please contact Michelle Lair, michellel@scientificsearch.com.
211,873 – Director of Commercial Analysis – 15+ years experience. Coordinate work with European Knowledge Center, located in London and India. Ensure timely delivery of standard market intelligence, secondary sales and Ad-Hoc reports across all business units. Created first GSK in Eastern Europe Data warehouse (Oracle) and state of the art front-end tool (Cognos) to combine and centralize all available data sources to extensively streamline and enhance reporting solution for all CIS countries. Define and manage project scope and deliverables in coordination with project stakeholders and senior management. For additional information on this exceptional candidate please contact Tom Terrill, tomt@scientificsearch.com.
177,415 – Director of Manufacturing – Results-driven and versatile manager with over 20 years of increasing responsibility in the pharmaceutical industry. Extensive production experience including in-depth knowledge of cGMP’s, FDA, OSHA, and DEA regulations within a manufacturing environment. Develop and execute optimization strategies for the manufacturing processes in alignment with Site objectives (i.e. increased reliability, reductions in cost, cycle-time and non-conformances). Specific responsibility for continuous improvement in the Manufacturing. For additional information on this exceptional candidate please contact Stu Bergen, sb@scientificsearch.com.
212,350 – Senior Project Manager – *Will consider consulting or temporary opportunities* Pharmaceutical operations leader with over 22 years of experience in solid dose, inhale insulin, potent compounds, controlled substances, sterile and consumer products. Project Management for the Coumadin Compliance Remediation Plan and Start of Commercial Manufacturing after commercial production stoppage due to compliance issues, recalls, field alerts and FDA Inspection. Managed all aspect of Coumadin manufacturing FDA remediation plan and return to commercial manufacturing. Department Head and Team Leader responsible of all the manufacturing and process engineering for the Pfizer Consumer plant in Puerto Rico, managing over 130 personnel. Restructured the manufacturing department organization to facilitate forecasted site and volume growth, improve efficiency and productivity, add manufacturing flexibility and leverage department resources. For additional information on this exceptional candidate please contact Caitlin Holton, caitlin@scientificsearch.com.
194,585 – Pharmacovigilance Associate – *Will consider consulting or temporary opportunities* 22 years experience. Responsible for the intake of adverse event information. Perform out bound follow up calls or write follow up letters to consumers and healthcare professionals. Data entry and MedDRA coding of adverse events into safety database. Support the creation and review of client specific work instructions. Maintained strict compliance to departmental and company SOPs. Addressed Medical Inquiries. Triaged the initial ADE/ADR for seriousness, completeness, and for coding. Maintained the PQC database and supporting documentation. For additional information on this exceptional candidate please contact Michelle Lair, michellel@scientificsearch.com.
