Pharmaceutical Industry Intern Job at Accreditation Council for Medical Affairs (ACMA) (Oradell, NJ)

Senior Manager, Global Medical Affairs (Menopause)

This role is pivotal in providing subject matter knowledge and expertise, develo...

Location

United Kingdom , London

Salary:

Not provided

Theramex

Expiration Date

Until further notice

Requirements

Medical degree with GMC registration or equivalent international qualification or Master of Pharmacy with GPhC registration
Previous experience in Medical Affairs, Clinical Research, or Pharmacovigilance within the pharmaceutical industry
Very good understanding of Medical Affairs’ role as scientific enabler and strategic partner in a pharmaceutical company
Strong knowledge and subject matter in women’s health
Ability to cut through scientific complexity and to communicate precisely and clearly with different target audiences
Strong interpersonal and leadership skills and track record of expertise working in a cross-functional environment
Strong analytical and strategic thinking
Strong business acumen
Highest professional work ethics
Proven knowledge of the ABPI Code of Practice and codes of international associations of the pharmaceutical industry, with experience in reviewing and/or certifying materials

Job Responsibility

Develop and implement medical plans aligned with business objectives and manage associated budgets
Provide expert medical input across the product lifecycle, including: Evidence generation
Evidence dissemination (e.g. health care professional education programs)
Medical experts’ engagement programs (e.g. advisory boards)
Build and maintain relationships with international therapy area experts and medical-scientific professional societies
Act as a medical reviewer for promotional and non-promotional materials in line with the ABPI and international associations of the pharmaceutical industry codes as well as internal SOPs
Support regulatory and market access submissions with clinical content
Ensure compliance with all relevant regulations and contribute to continuous process improvement
Ensure operational excellence

What we offer

A fast-paced environment, with broad exposure, where you can develop professionally – even outside your area of expertise
We support you as you grow and learn, and we love to celebrate success and recognize performance
We provide opportunities for driven and talented professionals who want to be part of our exciting journey

Manager, Clinical Operations, International

Cabaletta is seeking a Manager/Sr Manager, Clinical Operations, International. R...

Location

Germany; Switzerland

Salary:

Not provided

Cabaletta Bio Inc

Expiration Date

Until further notice

Requirements

Bachelor’s Degree or advanced degree in life sciences or related field
Minimum 4 years of clinical trial management experience including management of study resources, vendors, budgets, supplies, critical path activities, and risk management, within Biotech or pharmaceutical industry or equivalent by experience
Cell therapy experience preferred and/or focus complex therapies
Fluency in English
working proficiency in additional European languages a plus
Experience with early phase, complex trials
Experience managing Contract Research Organizations and other external vendors
Good understanding of European regulatory requirements (EMA, MHRA, etc)
Working knowledge of GCP/ ICH regulatory guidelines
Extensive knowledge of standard industry practices related to study start-up, site management and monitoring, document management, and clinical supply management

Job Responsibility

Provide day-to-day clinical project management oversight of the full range of clinical operations activities associated with clinical trial conduct from protocol development, feasibility/capability assessments, initiation, execution, control, and closure
Perform hands-on activities not outsourced to vendors, as needed
Author study documents and plans such as ICF and study specific plans
Provide input and review of site training materials
Review and provide clinical operations input into relevant clinical documents such as the protocol, investigator brochure, regulatory documents, clinical study reports and other documents and plans as appropriate
Proactively identify risks and lead team members to mitigate risks in a timely fashion
Develop and maintain positive relationships, both internal and external to project, including site personnel (KOLs, PIs, Study Coordinators)
Select and manage vendors
Perform and document study-level Sponsor Oversight of outsourced clinical activities
Execute clinical operations country submission tasks and documents: Review submission pack, coordinate country-specific ethics RFIs, review and update site-specific consent forms

What we offer

health and retirement
PTO
stock option plans

Senior Quality Assurance Manager

The Senior Quality Assurance Manager is responsible for assuring conformity of t...

Location

Belgium , Lessines

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a relevant scientific discipline
advanced degree preferred
Minimum of 10 years of experience within the pharmaceutical industry, with progressively increasing levels of responsibility
Minimum 5 years of experience in people management
Fluency in French and English is a must
Being recognized as Qualified Person, as defined in the Directive 2001/83/EC for Medicinal products and as defined in DIRECTIVE 2001/82/EC for veterinary medicinal products is an added value
Problem-solving and analytical skills
Critical and inquisitive mind
Excellent communication and presentation skills
Resistant to stress & demonstration of flexibility in times of change.

Job Responsibility

Supervising all activities at plant level as related to Operational Quality, Complaints and Release
Assure escalation of any potential FA and gather data to assist FA process
Support product release by ensuring timely review and investigation of deviations related to the manufacturing process
Support NCR and CAPA process: root cause identification and continuous improvement
Ensure timely documentation and closure of NCR, CAPA and complaint records
Ensure timely investigation and response to ICARs
Review and assess process and documentation change requests
Participate in internal and external quality system audits conducted by the corporate or regulatory agency representatives
Collaborate with ICO partners for projects or issue resolution (intracompany)
Support quality systems by driving regulatory compliance and continuous improvement activities in accordance with applicable regulations and business goals and objectives

What we offer

Support for Parents
Continuing Education/Professional Development
Employee Health & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer.

Fulltime

Automation Manager

Responsible for the planning, implementation, operation, maintenance, optimizati...

Location

China , Shanghai

Salary:

450000.00 - 550000.00 CNY / Year

Randstad

Expiration Date

June 17, 2026

Requirements

Bachelor's degree or above in Automation, Electrical Engineering and Automation, Measurement and Control Technology and Instruments, Process Equipment and Control Engineering, or related majors
master’s degree preferred
Prior experience in foreign-invested pharmaceutical manufacturing enterprises preferred
familiarity with GMP and other compliance requirements in the pharmaceutical industry
experience in automation management in pharmaceutical facilities highly preferred
5-8+ years of experience in automation-related fields, including 3+ years in team management
experience in managing automation teams in pharmaceutical facilities preferred
Hands-on experience in O&M, optimization, and project management of automation systems (PLC, SCADA, MES, DCS, etc.)
experience in implementing automation projects on pharmaceutical production lines preferred
Experience participating in external regulatory inspections (NMPA, etc.) and internal audits

Job Responsibility

Responsible for the full lifecycle management of all automated equipment and control systems (such as PLC, SCADA, MES, DCS, BMS, EMS, etc.)
Ensure automation systems meet data integrity regulatory requirements
establish SOPs for routine data integrity maintenance
Develop daily operation and maintenance management systems, safety operating procedures, and emergency response plans for automation systems
Responsible for compliance management of automation systems
coordinate with internal audits and external regulatory inspections (EMEA, PIC/S, NMPA, etc.)
Responsible for the overall management of automation-related projects (such as automation setup for new production lines, upgrade and renovation of existing systems, introduction of intelligent equipment, etc.)
Monitor trends in automation and intelligent technologies in the pharmaceutical industry
propose optimization and upgrade recommendations for automation systems
Collaborate with Production, Quality Control, and Warehousing departments to optimize automation processes

Fulltime

Senior Vice President, Business Strategy

As our Senior Vice President, Business Strategy, you are the strategic sales lea...

Location

United States

Salary:

Not provided

Vaniam Group

Expiration Date

Until further notice

Requirements

Advanced Degree: PhD, PharmD, MD, MBA, MSN, ARNP, or a related degree preferred
A minimum of 15 years of healthcare experience
At least 5 years in the medical communications industry
Comprehensive experience in the pharmaceutical and biotech industries
Strong leadership skills, including experience managing teams
A polished presentation style with the ability to engage audiences
Solutions-oriented problem-solving abilities
Effective Communication: Strong skills in negotiation, relationship-building, and conveying complex information
Technical Proficiency: Highly skilled in optimal CRM use, MS Office (Word, Excel, PowerPoint, Outlook), Adobe Acrobat, Chrome/Firefox, Egnyte/Dropbox, and Zoom
Willingness to travel within the US and internationally based on project and business needs (up to 60% travel expected)

Job Responsibility

Deliver growth aligned to Vaniam Group’s annual strategy, budget, forecast, and KPIs
Collaborate to develop the Vaniam growth strategy
Develop, lead, and/or support presentations to prospective and existing clients, securing new business opportunities
Ensure all customer-facing assets align with client objectives and therapeutic priorities
Lead, manage, and develop the business strategy team to achieve strategic goals
Develop sales targets for each business strategy team member
Provide mentorship to drive performance, professional growth, and alignment with organizational objectives
Manage business development processes, including sales forecasts and reports
Build strong client relationships and establish Vaniam Group as both a strategic partner and industry expert
Partner across internal teams to incubate and promote innovative capabilities

What we offer

100% remote environment with opportunities for local meetups
Positive, diverse, and supportive culture
Investment in you with opportunities for professional growth and personal development through Vaniam Group University
Health benefits – medical, dental, vision
Generous parental leave benefit
Focused on your financial future with a 401(k) plan and company match
Work-life balance and flexibility
Flexible time off policy for rest and relaxation
Volunteer time off for community involvement
Emphasis on personal wellness

Fulltime

Director, Validation

As a member of the Validation organization, the Validation Director will lead ph...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Bachelor’s degree in science or engineering required
15+ years of progressive leadership of operational validation experience in Pharmaceutical or Biotechnology industry, required
Sound industry knowledge of pharmaceutical and medical device facilities, lyophilization technology, cleanrooms, facilities clean utilities. WFI, purified water, process gasses, HVAC and industry processes and utilities
Experience in successful management of complex technical issues using structured analysis, methodology and articulates clear and concise direction to other operations staff
Strong experience with project and people management, particularly for large validation projects or programs
Experience in Facility, Equipment and Utility or Cleaning validation is a must (preferably in a multi-product CMO facility)
Demonstrate SME level knowledge of process/equipment validation, computer systems, standards and GxP regulations. Strong technical experience in the successful management of complex validation is required
Able to effectively lead and coordinate multiple, complex requests/projects and allocate resources effectively, across multiple sites, managing both local and remote based staff
Advanced understanding of applicable regulatory requirements (FDA, EMA, international regulatory)
Advanced understanding of industry standards for commissioning and validation of facilities, utilities and process equipment for cGMP manufacturing

Job Responsibility

Provide strategic and operational leadership to the Validation function, ensuring continuous, compliant execution of validation activities in alignment with established procedures, schedules, and business objectives
Evaluate process, equipment, and systems validation capabilities across Operations and develop short- and long-term improvement strategies to support corporate and regulatory goals
Guide the strategy for development, execution, review, and approval of all validation documentation, including IQ, OQ, and PQ protocols and reports
Ensure effective oversight of change control, deviations, investigations, and CAPAs related to validation activities
provide leadership in Quality Management System (QMS) integration and inspection readiness
Partner with senior leadership to define and implement validation strategies for new and existing processes, equipment, utilities, and systems, translating strategy into compliant protocols and SOPs
Direct and manage all aseptic and non-aseptic validation activities, including process validation, cleaning validation, sterilization validation, and equipment qualification
Maintain ownership and accountability for the site Master Validation Plan, ensuring alignment with regulatory expectations and business needs
Serve as a primary client and internal stakeholder interface for assigned validation projects, ensuring alignment on scope, timelines, and compliance requirements
Provide strategic leadership for validation-related regulatory inspections and third-party audits, including timely and effective closure of observations and commitments

Fulltime

Market Research and Forecasting Manager

Lead market research and forecasting for a dynamic oncology portfolio in a leadi...

Location

Japan , Tokyo

Salary:

10000000.00 - 13000000.00 JPY / Year

Randstad

Expiration Date

June 18, 2026

Requirements

Minimum 3 years of experience in market research or forecasting within the pharmaceutical industry
Master's degree or equivalent in a relevant field (e.g., Business, Life Sciences)
Proven experience in utilizing various market research methodologies (quantitative and qualitative)
Strong analytical skills with the ability to interpret complex datasets and extract key insights
Proficiency in Microsoft Excel, PowerPoint, and ideally Power BI
Excellent communication and presentation skills
Experience in the Oncology therapeutic area is highly desirable
Fluency in Japanese and business-level English is required
Experience managing multiple projects simultaneously
Understanding of pharmaceutical industry data sources (IQVIA, MDV, etc.) is a plus

Job Responsibility

Lead the development and maintenance of sales forecasting models for existing and future oncology products
Manage market research projects, from planning and execution to analysis and insightful presentation of findings
Collaborate with cross-functional teams (marketing, medical, etc.) to ensure alignment and the effective use of research
Synthesize complex data into actionable recommendations to inform strategic decisions
Contribute to competitive intelligence gathering and analysis
Identify and leverage key internal and external data sources to create robust forecasts

What we offer

健康保険
厚生年金保険
雇用保険
土曜日
日曜日
祝日

Fulltime

Medical Science Liaison

To maximize Amgen's value propositions through first-class medical and scientifi...

Location

Japan , Tokyo

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Education history in life-science or relevant area
Minimum of 2 years in pharmaceutical industry, or proven industry collaboration in academia
Experience in Medical Department or Clinical Development, or relevant field
Knowledge in osteoporosis, orthopedics, other metabolic bone diseases
Good communication/negotiation skills with scientific experts and internal stakeholders

Job Responsibility

To identify, develop and maintain collaborative relationships with current and future scientific experts, cooperative study groups
To discuss scientific value messages, clinical outcome and patient benefits with scientific experts and opinion leaders
To work with Medical and relevant internal colleagues to create engagement plan for external experts
To provide insights from field activity and contribute to local medical and brand strategy activities for the product(s) in accordance with internal and external regulations
To identifies new research opportunities and provide support for Investigator Sponsored Studies (ISS) and Amgen Sponsored Trials, when necessary
To ensures society engagement: MSL support of international and regional congresses
To implements and disseminates high quality medical and scientific educational programs as well as managing the medical events to achieve those objectives, not only providing logistic supports
To support local operation of clinical trials in collaboration with cross-functional development team
To communicate with medical and other relevant organizations of alliance partners and maximize the value of collaboration
Participates in/conducts Local Advisory Board Meetings, Investigator Meetings and/or Expert Panels

Pharmaceutical Industry Intern

Accreditation Council for Medical Affairs (ACMA)

Location:
United States , Oradell, NJ

Category:
Pharmacy

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
December 05, 2025

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Pharmaceutical Industry Intern

Senior Manager, Global Medical Affairs (Menopause)