177 Pharmaceutical Manager jobs in the United States

Pharmaceutical Packaging Manager

22110 Manassas, Virginia Confidential

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Job Description

Job Title: Packaging Manager (1st, 2nd & 3rd Shift)

Location: Manassas, VA (On-Site)

Job Type: Full-Time


Shifts Available:

  • 1st Shift: 7:00 AM – 3:30 PM
  • 2nd Shift: 3:00 PM – 11:30 PM (typically 2:30 PM – 12:00 AM)
  • 3rd Shift: 11:00 PM – 7:30 AM (may vary based on business needs)


Position Overview

We are seeking an experienced Packaging Manager to oversee and lead pharmaceutical packaging operations across multiple shifts. The Packaging Manager will supervise line leads and operators, ensure compliance with cGMP regulations, and drive production efficiency while maintaining product quality and safety standards. This role requires strong leadership, technical knowledge of bottle packaging lines, and hands-on supervisory experience in a pharmaceutical or nutraceutical manufacturing environment.


Key Responsibilities

  • Plan, schedule, and execute packaging operations based on production requirements and equipment capacity.
  • Supervise, train, and mentor packaging operators and line leads on SOPs, cGMP, investigations, CAPAs, and safety standards.
  • Ensure compliance with FDA, OSHA, and internal manufacturing requirements.
  • Manage packaging documentation including protocols, validations, cleaning verification, and change controls.
  • Oversee deviation management, investigations, and timely CAPA implementation.
  • Ensure packaging records, reports, and ERP data entries are accurate and completed on time.
  • Support interviewing, hiring, and onboarding of packaging staff.
  • Monitor equipment performance and oversee cleaning verification and validation activities.
  • Partner with Quality, HR, Warehouse, and Supply Chain teams to align with company goals.
  • Promote safety, teamwork, and continuous improvement within the department.


Qualifications

  • Bachelor’s degree in Science, Pharmacy, or related field.
  • 8–10 years of packaging experience in pharmaceutical manufacturing.
  • Minimum 5–8 years supervisory experience in bottle packaging lines (oral solid dosage required).
  • Proven experience managing multiple packaging lines and staff.
  • Strong knowledge of cGMP, FDA regulations, and packaging compliance.
  • Hands-on experience with production planning and team leadership.
  • Experience interviewing and hiring packaging operators/line leads.
  • Strong organizational, problem-solving, and communication skills.
  • Must be flexible for 1st, 2nd, or 3rd shifts and willing to work overtime if needed.


Benefits

  • Competitive salary + shift differentials
  • Relocation support & temporary housing available
  • Full-time benefits (health, dental, vision, 401k match, PTO)
  • Career growth opportunities within a global pharmaceutical company
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Pharmaceutical Project Manager

29610 Greenville, South Carolina HTI

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Job Description

Job Summary

The Project Manager has the primary responsibility of coordinating and managing defined projects that support the commercial introduction of Private Label pharmaceutical liquid products. This role requires working closely with the internal cross functional team and Private Label customers to manage commercial preparation and launch activities. High level of customer service experience with customers as a front-line company representative is crucial for this role. This position will also be responsible for management of internal projects that support pharmaceutical product development, product transfers, internal/external new product commercialization, cost improvement, and compliance driven initiatives.


Duties and Responsibilities:

  1. Interacts directly with all Private Label customers and is responsible for assigned new product launch projects to ensure they are planned and executed on time, budget, and within scope. Private Label projects are planned, managed, and executed generally over a 6-month period while internal projects can have a lifespan of 6-months to 1.5-years.
  2. For Private Label Projects, works closely with Supply Chain, Quality, Commercial and Customer Service to assure a clean transition of responsibilities from new product launch to routine product orders and maintaining customer supply.
  3. Proactively assesses project risks, escalates issues, develops mitigation plans, removes bottlenecks and leads regular team meetings working cross functionally with departments as needed in the organization to ensure completion of project deliverables.
  4. Uses project management tools and methodology to develop project plans, meeting minutes, etc. that are shared with clients, team members and management.
  5. Acts as a point of contact for project reporting and updating. Tracks projects and provides timely/relevant project updates to project team, management team and stakeholders.
  6. Develops presentation materials and aids in leading teams through project reviews.
  7. Develops, manages, and closes project change control documents on time.
  8. Responsible for communicating with upper management and other departments on a consistence basis regarding projects, status updates, issues, and recommendations.
  9. Performs other duties as assigned.


Required Skills/Abilities:

  • Individual must be organized, detail-oriented, and self-motivated.
  • Decision making, communication and planning.
  • Experience with R&D Teams, Direct interface with customers
  • Pharmaceutical, Nutritional and Food manufacturing preferred.


Education and Experience:

  • Bachelor’s degree in science or engineering is preferred
  • 1-3 years of experience in project management, preferably in the pharmaceutical or related industry.
  • Understanding of GMP (Good Manufacturing Practices) requirements in the pharmaceutical industry.
  • Strong organizational skills with the ability to manage multiple projects simultaneously.
  • Proficiency in SAP, Trackwise, and MS Office.
  • Previous experience with customer service within pharmaceutical and food manufacturing is desired.
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Pharmaceutical Project Manager

08902 North Brunswick, New Jersey Ascendia Pharmaceutical Solutions

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Job Description

About Ascendia Pharmaceutical Solutions:


Ascendia is a Contract Development and Manufacturing Organization (CDMO) company dedicated to enabling formulations for pre-clinical and clinical stage drug candidates and developing enhanced formulations of existing drug products. Ascendia specializes in creating formulations for poorly-water soluble molecules using nano-particle technologies. Ascendia assesses the feasibility of a broad array of formulation options in order to improve a drug’s bioavailability and solubility. Ascendia’s technologies include nano-emulsions, amorphous solid dispersions, nano-milling, injectable, lipid nanoparticles, and oral controlled release. Ascendia provides development, manufacturing and testing services - from discovery-stage molecules to life-cycle-management projects - creating formulation solutions with enhanced biopharmaceutical properties suitable for clinical scale-up.

The mission of our company is to provide customized formulation solutions to “salvage” difficult compounds and to create advanced medicines to help patients “prevail” over their disease and enhance quality of life.


About the Position:

Job Summary:

We are looking for a highly skilled and detail-oriented Pharmaceutical Project Manager to support the management and execution of pharmaceutical R&D and cGMP drug product manufacturing projects. In this role, you will assist in creating and updating project timelines, manage agendas and meeting minutes, source necessary resources and materials, and track the progress of project deliverables. The ideal candidate will be proactive and have excellent organizational skills, attention to detail, and experience in project management within the pharmaceutical or healthcare sectors.



Key Responsibilities:

  • Project Coordination:
  • Assist with the creation and management of detailed project timelines, tracking milestones, and ensuring all deliverables are completed on time.
  • Meeting Management:
  • Coordinate project meetings, prepare agendas, ensure relevant stakeholders are invited, and take clear and concise meeting minutes. Follow up on action items to ensure timely completion.
  • Sourcing & Vendor Management:
  • Support the sourcing of materials, vendors, and other resources required for the project. Work with cross-functional teams to ensure the timely procurement of required resources.
  • Documentation & Reporting:
  • Ensure that all project documentation is up-to-date and easily accessible. Track and report on the status of project deliverables, including any potential risks or delays.
  • Stakeholder Communication:
  • Communicate regularly with internal and external stakeholders to provide updates on project status, resolve issues, and ensure alignment on project goals and timelines.
  • Quality Control:
  • Monitor the project’s progress and performance, identifying and addressing any gaps or issues. Ensure all activities are compliant with industry regulations and quality standards.
  • Process Improvement:
  • Identify opportunities for process improvements and work with the team to implement more efficient project management strategies.
  • Business Development

Ensure timely generation of scopes of work from existing clients garnering feedback from relevant stakeholders.



Qualifications:

  • Education:
  • Bachelor’s degree in Pharmaceutical Sciences, Business, Project Management, or a related scientific field. PMP certification or equivalent is a plus.
  • Experience:
  • 1-3+ years of experience in pharmaceutical project management or a similar role, with proven ability to manage cross-functional teams and multiple projects simultaneously.
  • Skills:
  • Knowledge of pharmaceutical industry regulations and standards is strongly preferred. Project management experience in a CDMO environment is a plus.
  • Strong organizational and time-management skills.
  • Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and project management tools (e.g., MS Project, Trello, Asana).
  • Excellent written and verbal communication skills.
  • Ability to work independently and handle multiple tasks simultaneously.
  • Strong attention to detail and problem-solving abilities.
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Pharmaceutical Packaging Manager

Manassas, Virginia Confidential

Posted today

Job Viewed

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Job Description

Job Title: Packaging Manager (1st, 2nd & 3rd Shift)

Location: Manassas, VA (On-Site)

Job Type: Full-Time

Shifts Available:

  • 1st Shift: 7:00 AM – 3:30 PM
  • 2nd Shift: 3:00 PM – 11:30 PM (typically 2:30 PM – 12:00 AM)
  • 3rd Shift: 11:00 PM – 7:30 AM (may vary based on business needs)

Position Overview

We are seeking an experienced Packaging Manager to oversee and lead pharmaceutical packaging operations across multiple shifts. The Packaging Manager will supervise line leads and operators, ensure compliance with cGMP regulations, and drive production efficiency while maintaining product quality and safety standards. This role requires strong leadership, technical knowledge of bottle packaging lines, and hands-on supervisory experience in a pharmaceutical or nutraceutical manufacturing environment.

Key Responsibilities

  • Plan, schedule, and execute packaging operations based on production requirements and equipment capacity.
  • Supervise, train, and mentor packaging operators and line leads on SOPs, cGMP, investigations, CAPAs, and safety standards.
  • Ensure compliance with FDA, OSHA, and internal manufacturing requirements.
  • Manage packaging documentation including protocols, validations, cleaning verification, and change controls.
  • Oversee deviation management, investigations, and timely CAPA implementation.
  • Ensure packaging records, reports, and ERP data entries are accurate and completed on time.
  • Support interviewing, hiring, and onboarding of packaging staff.
  • Monitor equipment performance and oversee cleaning verification and validation activities.
  • Partner with Quality, HR, Warehouse, and Supply Chain teams to align with company goals.
  • Promote safety, teamwork, and continuous improvement within the department.

Qualifications

  • Bachelor’s degree in Science, Pharmacy, or related field.
  • 8–10 years of packaging experience in pharmaceutical manufacturing.
  • Minimum 5–8 years supervisory experience in bottle packaging lines (oral solid dosage required).
  • Proven experience managing multiple packaging lines and staff.
  • Strong knowledge of cGMP, FDA regulations, and packaging compliance.
  • Hands-on experience with production planning and team leadership.
  • Experience interviewing and hiring packaging operators/line leads.
  • Strong organizational, problem-solving, and communication skills.
  • Must be flexible for 1st, 2nd, or 3rd shifts and willing to work overtime if needed.

Benefits

  • Competitive salary + shift differentials
  • Relocation support & temporary housing available
  • Full-time benefits (health, dental, vision, 401k match, PTO)
  • Career growth opportunities within a global pharmaceutical company

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Pharmaceutical Packaging Manager (Manassas)

22110 Manassas, Virginia Confidential

Posted 1 day ago

Job Viewed

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Job Description

part time

Job Title: Packaging Manager (1st, 2nd & 3rd Shift)

Location: Manassas, VA (On-Site)

Job Type: Full-Time


Shifts Available:

  • 1st Shift: 7:00 AM 3:30 PM
  • 2nd Shift: 3:00 PM 11:30 PM (typically 2:30 PM 12:00 AM)
  • 3rd Shift: 11:00 PM 7:30 AM (may vary based on business needs)


Position Overview

We are seeking an experienced Packaging Manager to oversee and lead pharmaceutical packaging operations across multiple shifts. The Packaging Manager will supervise line leads and operators, ensure compliance with cGMP regulations, and drive production efficiency while maintaining product quality and safety standards. This role requires strong leadership, technical knowledge of bottle packaging lines, and hands-on supervisory experience in a pharmaceutical or nutraceutical manufacturing environment.


Key Responsibilities

  • Plan, schedule, and execute packaging operations based on production requirements and equipment capacity.
  • Supervise, train, and mentor packaging operators and line leads on SOPs, cGMP, investigations, CAPAs, and safety standards.
  • Ensure compliance with FDA, OSHA, and internal manufacturing requirements.
  • Manage packaging documentation including protocols, validations, cleaning verification, and change controls.
  • Oversee deviation management, investigations, and timely CAPA implementation.
  • Ensure packaging records, reports, and ERP data entries are accurate and completed on time.
  • Support interviewing, hiring, and onboarding of packaging staff.
  • Monitor equipment performance and oversee cleaning verification and validation activities.
  • Partner with Quality, HR, Warehouse, and Supply Chain teams to align with company goals.
  • Promote safety, teamwork, and continuous improvement within the department.


Qualifications

  • Bachelors degree in Science, Pharmacy, or related field.
  • 810 years of packaging experience in pharmaceutical manufacturing.
  • Minimum 58 years supervisory experience in bottle packaging lines (oral solid dosage required).
  • Proven experience managing multiple packaging lines and staff.
  • Strong knowledge of cGMP, FDA regulations, and packaging compliance.
  • Hands-on experience with production planning and team leadership.
  • Experience interviewing and hiring packaging operators/line leads.
  • Strong organizational, problem-solving, and communication skills.
  • Must be flexible for 1st, 2nd, or 3rd shifts and willing to work overtime if needed.


Benefits

  • Competitive salary + shift differentials
  • Relocation support & temporary housing available
  • Full-time benefits (health, dental, vision, 401k match, PTO)
  • Career growth opportunities within a global pharmaceutical company
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Pharmaceutical Project Manager (North Brunswick)

08902 North Brunswick, New Jersey Ascendia Pharmaceutical Solutions

Posted 1 day ago

Job Viewed

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Job Description

part time

About Ascendia Pharmaceutical Solutions:


Ascendia is a Contract Development and Manufacturing Organization (CDMO) company dedicated to enabling formulations for pre-clinical and clinical stage drug candidates and developing enhanced formulations of existing drug products. Ascendia specializes in creating formulations for poorly-water soluble molecules using nano-particle technologies. Ascendia assesses the feasibility of a broad array of formulation options in order to improve a drugs bioavailability and solubility. Ascendias technologies include nano-emulsions, amorphous solid dispersions, nano-milling, injectable, lipid nanoparticles, and oral controlled release. Ascendia provides development, manufacturing and testing services - from discovery-stage molecules to life-cycle-management projects - creating formulation solutions with enhanced biopharmaceutical properties suitable for clinical scale-up.

The mission of our company is to provide customized formulation solutions to salvage difficult compounds and to create advanced medicines to help patients prevail over their disease and enhance quality of life.


About the Position:

Job Summary:

We are looking for a highly skilled and detail-oriented Pharmaceutical Project Manager to support the management and execution of pharmaceutical R&D and cGMP drug product manufacturing projects. In this role, you will assist in creating and updating project timelines, manage agendas and meeting minutes, source necessary resources and materials, and track the progress of project deliverables. The ideal candidate will be proactive and have excellent organizational skills, attention to detail, and experience in project management within the pharmaceutical or healthcare sectors.



Key Responsibilities:

  • Project Coordination:
  • Assist with the creation and management of detailed project timelines, tracking milestones, and ensuring all deliverables are completed on time.
  • Meeting Management:
  • Coordinate project meetings, prepare agendas, ensure relevant stakeholders are invited, and take clear and concise meeting minutes. Follow up on action items to ensure timely completion.
  • Sourcing & Vendor Management:
  • Support the sourcing of materials, vendors, and other resources required for the project. Work with cross-functional teams to ensure the timely procurement of required resources.
  • Documentation & Reporting:
  • Ensure that all project documentation is up-to-date and easily accessible. Track and report on the status of project deliverables, including any potential risks or delays.
  • Stakeholder Communication:
  • Communicate regularly with internal and external stakeholders to provide updates on project status, resolve issues, and ensure alignment on project goals and timelines.
  • Quality Control:
  • Monitor the projects progress and performance, identifying and addressing any gaps or issues. Ensure all activities are compliant with industry regulations and quality standards.
  • Process Improvement:
  • Identify opportunities for process improvements and work with the team to implement more efficient project management strategies.
  • Business Development

Ensure timely generation of scopes of work from existing clients garnering feedback from relevant stakeholders.



Qualifications:

  • Education:
  • Bachelors degree in Pharmaceutical Sciences, Business, Project Management, or a related scientific field. PMP certification or equivalent is a plus.
  • Experience:
  • 1-3+ years of experience in pharmaceutical project management or a similar role, with proven ability to manage cross-functional teams and multiple projects simultaneously.
  • Skills:
  • Knowledge of pharmaceutical industry regulations and standards is strongly preferred. Project management experience in a CDMO environment is a plus.
  • Strong organizational and time-management skills.
  • Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and project management tools (e.g., MS Project, Trello, Asana).
  • Excellent written and verbal communication skills.
  • Ability to work independently and handle multiple tasks simultaneously.
  • Strong attention to detail and problem-solving abilities.
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Manager, Pharmaceutical Operations

03110 Bedford, New Hampshire PCI Pharma Services

Posted 1 day ago

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Job Description

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. **We are PCI.** Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. **Summary of Objective:** The Manager, Pharmaceutical Operations leads all aspects of manufacturing operations per assigned location and product type. Managers may work in medical device manufacturing or may support the manufacturing of drug products. The Manager may support aseptic, non-aseptic operation activities as well as lyophilization activities. As assigned, the manufacturing manager will be responsible for activities such as component preparation, product formulation, aseptic filling, stoppering, capping and lyophilization activities. The incumbent is also expected to support media fill activities and aseptic qualifications, audits, validation assistance, and the ability to maintain a cGMP environment, as well as participate in responses to internal and external audits. Manage formulation cleaning/decontamination, assembly, sterilization, high-level disinfection and distribution. Manages inventory and supplies supporting departmental activities. The manager is also tasked with developing and ensuring compliance with departmental budget, and to work collaboratively with other departments to create and ensure process and cost efficiencies. Excels in customer service, ensuring the highest standards for both internal and external customer satisfaction. **Essential Duties and Responsibilities:** + Responsible for managing and directing staff to ensure proper and continuous function of all manufacturing operations and adherence to the established schedules + Leads the safety initiatives for manufacturing and ensure department compliance with all PCI safety procedures, processes. + Ensures that all operations of the drug/product cleanroom areas are being performed in accordance with cGMP and current regulatory guidelines as well as all applicable SOPs + Supports the production schedule to meet requirements for staffing, work schedules, planning activities, and equipment maintenance + Directs personnel to complete and review all associated batch record and SOP documentation + Writes, reviews/approves investigation, OOT/OOS, EEIs and completion of deviation reports + Writes, reviews/approves change control orders and CAPAs + Coordinates assistance for Validation protocols, and other process studies. Coordinates activities for process enhancement projects and supports new product development projects + Ensures training of operators to learn techniques for product formulation, preparation of materials/products, aseptic technique, contamination control, gowning, , labeling and packaging + Oversees control of product manufacturing operation areas including cleanrooms, component prep and sanitization, filling, and packaging activities + Works closely with Validations, Facilities, Quality, Project Management and Senior Management to ensure the needs of all functions are met + Other duties as assigned, or as business needs require **Work Environment:** + Proficiency in pharmaceutical process development for aseptically produced products or medical device manufacture + Working knowledge of pharmaceutical facilities, lyophilization technology and manufacturing equipment as well as cleanrooms + Strong troubleshooting and root cause analysis skills + Able to effectively lead and coordinate multiple, complex requests/projects and allocate resources effectively + Able to effectively deal with complex technical issues using structured analysis, methodology and articulates clear and concise direction to other operations staff + Excellent oral and written (reports) communication skills + Strong organization and leadership skills + Self-motivated with a drive for excellence; able to inspire and motivate the staff + Honesty, integrity, respect and courtesy with all colleagues + Creative and can work with minimal supervision following internal procedures balanced with independent thinking + Resilient through operational and organizational change + Strong commitment to excellence and quality with a positive working attitude + This Manager will be responsible for the activities and schedules to meet designated timelines as well as communicating with the clients on technical aspects of the project, if needed. Additionally, this Manager will be responsible for communicating the status of the project with the rest of the organization including Manufacturing, Project Management, and the entire Quality team. + Responsible for revising and creating SOP's pertinent to daily tasks in PCI operations. Responsible for directing activities of Manufacturing Technicians. Assist in the preparation of staff evaluations. Must be able to observe and identify potential issues and address satisfactorily. + TRAVEL - <10% **Qualifications:** + BA science degree, or equivalent + A minimum of 5 years relevant pharmaceutical or medical device manufacturing experience + Proven aseptic process leadership experience + Must understand cGMP and WW regulatory requirements (e.g. EU) for parentals or familiar with working in ISO 5 and 6 areas. Gowning experience necessary. + Understanding of basic contamination and aseptic technique and any formal training would be beneficial. #LI-LL1 Join us and be part of building the bridge between life changing therapies and patients. Let's talk future ( **Equal Employment Opportunity (EEO) Statement:** _PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._ _At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture._ Why work for PCI Pharma Services? At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don't say no, we figure out how. PCI Pharma Services is an Equal Opportunity Employer/Vet/Disabled
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Warehouse Manager - Pharmaceutical Industry

19488 Norristown, Pennsylvania Ultimate Staffing

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Job Description

Oversee daily distribution center operations to ensure efficient, productive, and safe performance, while meeting customer service and business objectives. Maintain optimal functionality of facilities and equipment, and ensure compliance with corporate and regulatory directives. This is a direct hire opportunity that offers a base salary up to $100K + annual bonus (around $6K). This position is based in Norristown, PA


Job Duties:


  • Set standards for and supervise direct reports (Warehouse Manager and 2 team leads), as well as 55 indirect reports (warehouse associates).
  • Manage staffing needs, including hiring, training, motivating, and disciplining employees as necessary.
  • Collaborate with Warehouse Manager and Team Leaders to develop strategies and ensure all teams are aligned with customer needs.
  • Supervise the Warehouse Manager and Returns department, conducting performance reviews and addressing any performance issues.
  • Monitor financial and productivity metrics to achieve performance goals.
  • Communicate with sales teams regarding inventory and shipping concerns, and represent the branch in interactions with vendors and other branches.
  • Work with HR on payroll, hiring, terminations, and employee benefits.


Job Requirements:


  • 5 to 10 years of experience managing a distribution center (shipping, receiving, and picking).
  • At least two years of specialized training in warehouse management.
  • Veterinary industry experience is a plus.
  • Human Resources experience is desirable
  • Forklift certification or ability to obtain certification is required.
  • Ability to read and interpret safety rules, operating instructions, and procedural manuals.


All qualified applicants will receive consideration for employment without regard to race, color,

national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

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Pharmaceutical Distribution Center Manager

19488 Norristown, Pennsylvania Ultimate Staffing

Posted today

Job Viewed

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Job Description

Oversee daily distribution center operations to ensure efficient, productive, and safe performance, while meeting customer service and business objectives. Maintain optimal functionality of facilities and equipment, and ensure compliance with corporate and regulatory directives. This is a direct hire opportunity that offers a base salary up to $100K + annual bonus (around $6K). This position is based in Norristown, PA


Job Duties:

  • Lead daily operations of a high-volume distribution center, ensuring accurate and timely picking, packing, and shipping of around 2,000+ packages per day.
  • Monitor KPIs and financial metrics to drive productivity, cost efficiency, and service levels.
  • Supervise a Warehouse Manager, 2 Team Leads, and 60+ warehouse associates; set performance standards and conduct regular reviews.
  • Oversee staffing, including hiring, training, scheduling, and performance management to maintain a high-performing team.
  • Collaborate with warehouse leadership to align operations with customer expectations and seasonal demand.
  • Manage the Returns department and ensure efficient reverse logistics processes.
  • Partner with Sales and Inventory teams to resolve shipping and inventory issues.
  • Ensure compliance with safety standards and company policies.
  • Coordinate with HR on payroll, hiring, terminations, and employee relations.


Job Requirements:

  • 5 to 10 years of experience managing a distribution center (shipping, receiving, and picking).
  • At least two years of specialized training in warehouse management.
  • Pharmaceutical, surgical instruments, or medical devices industry experience is required
  • Human Resources experience is desirable
  • TEAM MENTALITY
  • Forklift certification or ability to obtain certification is required.
  • Ability to read and interpret safety rules, operating instructions, and procedural manuals.




All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

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Security Account Manager - Pharmaceutical

10591 Tarrytown, New York Allied Universal

Posted 1 day ago

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Job Description

**Company Overview:**
Allied Universal®, North America's leading security and facility services company, offers rewarding careers that provide you a sense of purpose. While working in a dynamic, welcoming, and collaborative workplace, you will be part of a team that contributes to a culture that positively impacts the communities and customers we serve. We offer a comprehensive benefits package that may include medical, dental, and vision coverage, life insurance, a retirement plan, employee assistance programs, company discounts, and other perks, depending on the position and eligibility.
**Job Description:**
Allied Universal® is hiring an Account Manager. As an Account Manager, you are the driving force behind daily security operations, ensuring the safety and well-being of the people and places you protect. You will lead from the front-guiding, developing, and motivating your team of security officers and supervisors to deliver exceptional service. This is your opportunity to lead with purpose, make a real impact, and create a safer environment for those who count on you.
**Why Join Allied Universal?**
+ **Career Growth:** Opportunities to advance within a global leader in security services
+ **Impactful Work:** Play a vital role in protecting people, property, and businesses
+ **Supportive Team:** Work with caring professionals dedicated to safety and excellence
**RESPONSIBILITIES:**
+ **Manage scheduling:** Leverage AI-powered technology to effectively schedule security officers, meeting client contract hours while minimizing unbilled overtime
+ **Lead and Develop Security Teams:** Hire, coach and manage security officers and supervisors while overseeing payroll, performance, and employee relations
+ **Enhance Client Relationships:** Serve as the primary point of contact for clients, ensuring high-quality service that protects people and property
+ **Handle Security Incidents and Emergencies:** Respond to escalated issues professionally, coordinating with clients and internal teams
+ **Direct Compliance and Security Operational Excellence:** Oversee training, safety, and site operational standards as well as managing inventory (uniforms, equipment, and other essential supplies)
**QUALIFICATIONS (MUST HAVE):**
+ High school diploma or equivalent
+ Licensing requirements are subject to state and/or local laws and regulations and may be required prior to employment
+ Valid driver's license if driving a company vehicle, or personal vehicle while conducting business
+ Minimum of two (2) years of experience in business operations, security management, or supervising teams in a fast-paced environment
+ Experience in leading, developing, and retaining a dynamic team while building positive client relationships
+ Knowledge of emergency preparedness, physical security protocols, risk assessments, and law enforcement coordination
+ Proven ability to evaluate situations, make sound independent decisions, and resolve conflicts in an efficient manner
+ Proficiency in web-based applications and computer systems, including Microsoft Office
+ Ability to communicate effectively with clients and employees while managing multiple projects and driving operational excellence
+ Financial acumen; able to manage staffing levels while minimizing non-billed overtime and managing turnover costs; planning and organizing skills to control costs related to inventory (uniforms, equipment, etc.)
**PREFERRED QUALIFICATIONS (NICE TO HAVE):**
+ College degree in Business Administration or a law enforcement-related field
+ Law enforcement, military, and/or contract or proprietary security services, or facility management experience
+ American Society of Industrial Security (ASIS), International Certified Protection Professional (CPP) certification
+ Previous payroll, billing, or scheduling experience
+ Aptitude with security systems: CCTV, access control, and badge administration
+ Graduate of certified public safety academy (e.g., Law Enforcement, Firefighter/Paramedic, Corrections Officer)
**BENEFITS:**
+ Medical, dental, vision, basic life, AD&D, and disability insurance
+ Enrollment in our company's 401(k)plan, subject to eligibility requirements
+ Eight paid holidays annually, five sick days, and four personal days
+ Vacation time offered at an accrual rate of 3.08 hours biweekly. Unused vacation is only paid out where required by law.
Salary: $85,696 / year
Allied Universal® is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race/ethnicity, age, color, religion, sex, sexual orientation, gender identity, national origin, genetic information, disability, protected veteran status or relationship/association with a protected veteran, or any other basis or characteristic protected by law. For more information: you have any questions regarding Equal Employment Opportunity, have difficulty using the online system and require an alternate method to apply, or require an accommodation at any time during the recruitment and/or employment process, please contact our local Human Resources department. To find an office near you, please visit: Universal® is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race/ethnicity, age, color, religion, sex, sexual orientation, gender identity, national origin, genetic information, disability, protected veteran status or relationship/association with a protected veteran, or any other basis or characteristic protected by law. For more information: you have any questions regarding Equal Employment Opportunity, have difficulty using the online system and require an alternate method to apply, or require an accommodation at any time during the recruitment and/or employment process, please contact our local Human Resources department. To find an office near you, please visit: ID:**
**Location:** United States-New York-Sleepy Hollow
**Job Category:** Account Manager, Management
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