Scientific Search specializes in Scientific Recruiting and staffing for a broad spectrum of positions across multiple industries such as Pharmaceutical, Medical Device, Instrumentation, Food, Chemical, Petroleum and Consumer Products. We have a dedicated Scientific 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 basic research, applied research, product development, packaging, quality control, engineering, operations, regulatory affairs and market research. Call or email us today and let us show you what our Scientific Recruiting team can do!
Our internal database contains thousands of qualified professionals that our Scientific 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 Scientific Candidates
88,303 – Regulatory Affairs Associate – Over 10 years experience. ANDAs preparation for FDA submission. Preparation of Amendments, Supplements, and Annual reports for FDA submission. Preparation and review of CMC documentation for ANDA preparation. Review FDA correspondence and submit required elements for response. Preparation and submission of post marketing safety reports such as quarterly ADE reports and yearly ADE reports. Preparation of Field Alert Report for FDA submission. Handling of Recall for marketed products. Preparation of labeling SPL for drug listing on DailyMed website. Maintains Compliance with regulatory requirements for generic drugs for the U.S market. MS – Drug Regulatory Affairs. For additional information on this exceptional candidate please contact Joe Peters, email@example.com.
237,814 – Director of Operations – *Will consider consulting or temporary opportunities* 22 years experience in Operations Management. Managed the reorganization and daily activities of a 75,000 sq ft packaging facilities servicing pharmaceutical, cosmetic and food and beverage industries. Develop effective Key Performance Indicators (KPIs) to sharpen daily, weekly and monthly production parameters in an effort to proactively manage customer expectations. Identify cost saving solutions (transportation, automation or labor reduction) to improve market competitiveness on an ongoing basis. Forecasted and procured all necessary materials, both vendor supplied and purchased. Schedule, prepare and monitor daily activities with 25 staff members within all departments, prioritizing operations to ensure meeting customer targets in a very dynamic environment. Participated in both customer and regulatory audits relative to quality, safety and security. BS – Business management. For additional information on this exceptional candidate please contact Jeff Boyle, firstname.lastname@example.org.
159,187 – Director, Pharmaceutical Manufacturing – Diverse career at premier global companies. Expertise spans Commercialization, Process Development, Supply Chain Management, and Product Lifecycle Management. Extensive experience leading and executing late stage development and commercialization of solid oral dosage forms while at Merck. International project leadership experience in matrix environments for both mature and emerging markets. Skilled manager with CMOs, suppliers, licensors, subsidiaries, business partners, acquisitions, and divestitures. Commercialized four products in US as well as major and emerging European, Latin American, and Asian markets. Built and managed collaborative, cross-functional relationships in areas where, due to increased therapeutic focus, many staff were new to Merck culture and approach. Facilitated at least 10 different product teams. MBA; BS – Chemical Engineering. For additional information on this exceptional candidate please contact Joe Peters, email@example.com.
236,872 – Quality Control Supervisor – Manage and maintain the company’s Quality System. Analyze process and lead the continuous improvement program including AIB Certification and Kosher Certification. Manage facility wide GMP Program and HACCP Program. Responsible for all in-house food safety, GMP audits. Experience overseeing 25+ employees. Responsible for all production entry information and line performance. Inspect all incoming raw product against product spec sheets. Manage inventory of all raw material, production supplies and packing material. Ensure subordinate staff is motivated to improve the efficiency of their current duties. Calibrate all lab machines. Responsible for weekly micro testing. Responsible for weekly manning schedules. Responsible for entering daily production numbers, opening and closing work orders in WMS. For additional information on this exceptional candidate please contact Kim Laipple, firstname.lastname@example.org.
217,370 – Senior Director, Chemistry and Manufacturing Services – *Will consider consulting or temporary opportunities* 20 years experience. Created, staffed, developed, and led a team of 3 directors and manager, 14 professional and line staff and managed $7M annual operating budget. Provided technology transfer, process engineering, continuous improvement, process validation, scale up, product commercialization, Lean Six Sigma (DMAIC), QbD, root cause analysis, and ongoing commercial verification expertise to company. Championed the training, mentorship, and projects for the successful deployment of a Lean Six Sigma rollout yielding 11 Black Belts in 4 departments. Reduced expenses and increased margins by leading a team of Six Sigma professionals on track to save $4.4M annually. Established an ongoing program of continued process verifications for commercial products to meet the FDA Process Validation Guidance, Stage 3 (2011, rev 1). Met corporate time frame requirements by directing 31 process validations with a staff of 4 in one year. BS – Pharmacy. BS – Chemical Engineering. For additional information on this exceptional candidate please contact Joe Peters, email@example.com.
233,787 – Senior Director, Engineering & Instrumentation – 10+ years in an Automated Process Control Environment 20+ years diverse experience working with Instrumentation, Electronic Controls equipment, PLC.s, etc. Supervisor and administration of daily work activities for the I/E maintenance department and also perform and document maintenance, calibration, installation, fault diagnosis, and repair of electrical, mechanical and pneumatic instruments and systems including PLCs, VFDs, HMIs & DCS control system. Substantial experience in project engineering such as qualifications/validations/commissioning of Pharma manufacturing equipment, facilities, and systems. Also extensive experience in environmental and safety compliance. Coordinate and supervise Electrical/Instrument group, as well as contractor and vendor activities relating to electrical, instrumentation and controls. Managed teams of 60+. Numerous licenses and certifications. For additional information on this exceptional candidate please contact John Barry, firstname.lastname@example.org.