DeltaMed Solutions, Inc.

Hello LinkedIn Connections! We are still looking and actively recruiting for a QA Specialist I position here at DeltaMed Solutions. The opportunity is open and we're eager to welcome qualified candidates to join our team! If you are interested, send your resume to [email protected]! Please see job description below for details: ***NOTE: Please only apply if you currently reside in NJ*** Responsibilities: - Support the design, implementation, and improvement of company quality standards in alignment with regulatory expectations. - Provide assistance in maintaining and updating Standard Operating Procedures (SOPs) and other key quality processes. - Support internal quality control audits, ensuring compliance with Good Clinical Practice (GCP) and regulatory standards. - Assist during external audits and inspections, ensuring proper documentation and compliance tracking. - Collaborate with teams to help develop and implement Corrective and Preventive Action Plans (CAPAs) in response to audit findings. - Monitor CAPA implementation, verifying their effectiveness in addressing identified quality gaps. - Participate in audit follow-up meetings, helping document findings and improvement timelines. - Help maintain accurate QA documentation, including audit reports, logs, and compliance records. - Assist in reviewing quality data trends to identify opportunities for improvement. - Support employee training efforts by assisting in organizing and maintaining compliance-related materials. - Generate basic reports and quality metrics to track progress and compliance. - Stay informed about industry trends and regulatory updates to enhance knowledge of quality and compliance standards. - Stay updated on regulatory changes in GCP, GDPR, FDA Guidelines and quality management to ensure ongoing compliance.. Qualifications: - BA or MS in Business or Science - 1-2 years' experience in a quality related field - Basic understanding of Good Clinical Practice (GCP) would be beneficial - Proficient PC skills including Microsoft Excel, Access, PowerPoint and Word is essential - Basic proficiency in Microsoft Office 365 (Excel, Word, PowerPoint, Outlook, Teams, and SharePoint) for documentation, reporting, and communication. - Eagerness to learn and develop skills in QA and regulatory compliance.

Hello LinkedIn Connections! We're delighted to announce that we are actively recruiting for a QA Specialist I position here at DeltaMed Solutions. The opportunity is open and we're eager to welcome qualified candidates to join our team! If you are interested, send your resume to [email protected]! Please see job description below for details: ***NOTE: Please only apply if you currently reside in NJ*** Responsibilities: - Support the design, implementation, and improvement of company quality standards in alignment with regulatory expectations. - Provide assistance in maintaining and updating Standard Operating Procedures (SOPs) and other key quality processes. - Support internal quality control audits, ensuring compliance with Good Clinical Practice (GCP) and regulatory standards. - Assist during external audits and inspections, ensuring proper documentation and compliance tracking. - Collaborate with teams to help develop and implement Corrective and Preventive Action Plans (CAPAs) in response to audit findings. - Monitor CAPA implementation, verifying their effectiveness in addressing identified quality gaps. - Participate in audit follow-up meetings, helping document findings and improvement timelines. - Help maintain accurate QA documentation, including audit reports, logs, and compliance records. - Assist in reviewing quality data trends to identify opportunities for improvement. - Support employee training efforts by assisting in organizing and maintaining compliance-related materials. - Generate basic reports and quality metrics to track progress and compliance. - Stay informed about industry trends and regulatory updates to enhance knowledge of quality and compliance standards. - Stay updated on regulatory changes in GCP, GDPR, FDA Guidelines and quality management to ensure ongoing compliance.. Qualifications: - BA or MS in Business or Science - 1-2 years' experience in a quality related field - Basic understanding of Good Clinical Practice (GCP) would be beneficial - Proficient PC skills including Microsoft Excel, Access, PowerPoint and Word is essential - Basic proficiency in Microsoft Office 365 (Excel, Word, PowerPoint, Outlook, Teams, and SharePoint) for documentation, reporting, and communication. - Eagerness to learn and develop skills in QA and regulatory compliance. #CRO #QualityAssurance #pharmajobs

As the year comes to a close, we want to thank our amazing clients for your continued trust and partnership. Your support has been key to our success, and we’re excited for what lies ahead in 2025! Wishing you a joyful and prosperous holiday season with loved ones! #HappyHolidays #ThankYou #ClientAppreciation

Our team recently celebrated the holiday season with a wonderful banquet dinner, followed by a fun and team-building hatchet throwing activity the next day. It was a great way to unwind, reflect on the past year, and strengthen our team dynamic. Looking forward to what the new year will bring!

Hello LinkedIn Connections! We're delighted to announce we are ALSO #hiring for a FSP Portfolio Manager position for our Strategic Services team! The opportunity is open and we're eager to welcome qualified candidates to join our team! If you are interested, send your resume to [email protected]! Please see job description below for details: ?Responsibilities: - Serve as the primary point of contact for assigned FSP clients and manage day-to-day interactions. - Oversee contract execution, scope of work, and compliance with agreed terms. - Monitor key performance, service level agreements and metrics to evaluate FSP performance. - Identify areas of improvement and implement corrective actions when performance gaps arise. - Facilitate regular performance reviews and ensure continuous quality improvement. - Track project timelines, deliverables, and resource allocation to ensure goals are met. - Ensure FSP operations adhere to regulatory guidelines, company policies, and industry standards. - Facilitate clear communication and alignment between FSP teams and internal teams. - Provide updates to management on FSP performance, progress, and risks. ? Qualifications: - B.S or M.S. in Life Sciences, Business, Project Management or relevant field - 5+ years of experience managing vendor relationships, outsourcing or clinical operations in pharmaceutical/CRO or biotechnology industry - Proven expertise in FSP models within pharmaceutical, CRO, biotechnology, or related industries. - Strong project management and organizational skills. - Proficiency in contract and financial management. - Excellent interpersonal, negotiation, and communication skills. - Must work well independently and in a team environment - Exceptional written and verbal communication skills. #CRO #PortfolioManager #pharmajobs

Hello LinkedIn Connections! We're delighted to announce that we are #hiring for a Recruiting Specialist position for our Strategic Services team! The opportunity is open and we're eager to welcome qualified candidates to join our team! If you are interested, send your resume to [email protected]! Please see job description below for details: ?Responsibilities: - Identify, research, and source biometrics professionals including biostatisticians, statistical programmers, data managers, and other specialized roles in the clinical trial industry. - Full life cycle recruiting includes job posting, sourcing, networking, screening, setting up internal and client technical interviews, offers and negotiations. - Conduct initial screenings to assess skill and cultural fit for clients and organization. - Prepare credentials on candidate’s background to share with the client. Utilize innovative tools, platforms, and networks to build a robust talent pipeline. - Maintain and build candidate database for company. - Maintain accurate documentation and generate reports on recruitment metrics and performance. - Maintain candidate relationships and provide regular updates. - Stay informed about industry trends, salary benchmarks, and competitor hiring in biometrics and industry sector. - Attend and network with candidates at assigned industry conferences. ? Qualifications: - B.S or M.S. in Sales, Business Administration, Human Resources, Management, or relevant field - 3-5+ years of experience recruiting in the pharmaceutical/CRO or biotechnology industry - Ability to work under pressure and possess strong time management skills - Excellent interpersonal skills with the ability to build relationships and be persuasive when needed - Must work well independently and in a team environment - Exceptional written and verbal communication skill #CRO #RecruitingSpecialist #pharmajobs

As we reflect on this season of gratitude, we would like to extend our sincere thanks to our clients, partners, and dedicated team members! Your continued support and collaboration are invaluable, and we are grateful for the opportunity to work alongside such remarkable individuals and organizations. We wish you all a peaceful and joyful holiday filled with warmth and appreciation!

Hello LinkedIn Connections! We're delighted to announce that we are actively #recruiting for a QA Manager position here at DeltaMed Solutions. The opportunity is open and we're eager to welcome qualified candidates to join our team! If you are interested, send your resume to [email protected]! Please see job description below for details: ***NOTE: Please only apply if you currently reside in NJ*** Responsibilities: - Design, implement and improve company quality standards. - Be responsible for company quality process including SOP and other working process. - Lead internal quality management including internal quality control audit. - Serve as primary point of contact and support for external audit and/or inspection. - Collaborate with teams to develop and implement corrective and preventive action plans (CAPAs) in response to audit findings. - Facilitate follow-up meetings with clients to discuss the findings, clarify any questions, and agree on timelines for implementing CAPAs. - Monitor the implementation of CAPAs and verify their effectiveness in addressing audit findings. - Prepare and present detailed audit reports to senior management, highlighting findings, recommendations, and follow-up actions. - Lead the preparation of comprehensive audit reports in response to client-initiated audits, ensuring findings are clearly documented, and evidence-based. - Analyze data in order to find areas for improvement. - Training, motivating, coaching, and correcting employees to ensure that standards are met. - Create reports to track progress. - Formulate strategies to increase productivity. - Review processes in order to ensure that they align with current trends. - Stay updated with changes in regulatory standards and guidelines to ensure ongoing compliance. Qualifications: - B.A. or M.S. in Business or Science - 3 to 5 years prior experience in a QA role - 2+ years of experience in industry of pharmaceutical, biotech, or CRO environment - Prior experience as an Assistant QA Manager is a plus - Excellent communication and writing skills, good people interact skills, proficient in MS-Word, Excel or other office/financial software - Willingness to assist other departments to develop solutions and metrics - Detail oriented #CRO #pharmaceuticalindustry #qualityassurance

???? We had a great time at our 2nd Annual Halloween Party! It was wonderful to see everyone’s creativity and team spirit. Thanks to everyone who joined in the fun! Check out our group photo from the night. ???? #DeltaMedSolutions #CRO #HalloweenFun

?? Yesterday was a blast as we celebrated Bring Your Child to Work Day at DeltaMed Solutions! From coloring to bingo, it was a day of fun for our team and their children. #BringYourChildtoWorkDay ??