채용
Purpose
Describe the primary goals, objectives or functions or outputs of this position.
- The role of the Manufacturing Supervisor II has knowledge and experience in its field while still building expertise. Is expected to work autonomously with little or no direct supervision. Lead and facilitate safe operations in line with all safety, regulatory and operational requirements.
- Assure the long-term effectiveness of the team: deliver high levels of customer service, ensure quality of product and services, comply with all regulatory requirements, achieve desired financial performance including cost reductions, and build a culture of high performance for the team.
Responsibilities:
List up to 10 main responsibilities for the job. Include information about the accountability and scope.
- Safety: Create an environment where safety is the number one priority in every activity that you do, driving safety improvements and conducting safety gembas routinely. Be present on the floor promoting a culture of zero safety incidents in compliance with all EHS requirements.
- People: Responsible for daily effective deployment of team members and ensure tasks are appropriately delegated to meet the production schedule. Ensure that team members are trained to the required standards of their job. Drives engagement with team by having regular 1:1s, conducts performance reviews and has survey actions plans in place. Ensure time and attendance is approved on time each week so that employees are paid correctly. Communicating effectively with team cascading important info.
- Operational: Provides assistance in developing weekly goals and production schedules to determine unit assignments and critical actions with little or no supervision. Responsible for the effective coordination of the activities within the shift to meet the production schedule. Ensure a smooth shift handover with the next manager to ensure departmental activities are planned and executed safely.
- Compliance: Ensure compliance with applicable regulatory agencies. Implement a proactive compliance management process where material checks, line clearance checks and spot checks are conducted routinely. Effectively manage any compliance issue that arises during shift that could potentially impact on lot completion.
- Performance: Responsible for change-over time management and complete cycle time management. Continuously seeks to identify improvements and supports the implementation of process improvement projects.
Responsible for managing resources across all of production to maximize shift throughput.
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Accountable for overall shift training program (where applicable).Knows all metrics and actively supports initiatives to ensure their area meets expectations and targets.
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Development: Be proactive in self-development by having a growth mindset towards personal development.
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Ensures all employees in their organization have development action/ plans in place and arranging opportunities for growth.
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Operation Excellence (Op Ex): Participates in process improvement initiatives.
Qualifications:
List required and preferred qualifications (up to 10). Include education, skills and experience.
- Bachelor’s degree is required. A degree in sciences or engineering is preferred. A minimum 2 years experience supervising or leading a functional team. Experience in regulated pharmaceutical industry is strongly preferred.
- Experience: Systems
- Proficient in Microsoft Office and other manufacturing systems, such as SAP. Familiarity with industrial automation (distributed control and PLC based systems). Experience in cross functional process improvement initiatives is preferred.
- Experience: Regulatory- Working knowledge of safety, quality systems, and cGMPs is required.
- Experience: Aseptic (If applicable) -Experience working in an aseptic production environment preferred.
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
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The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
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We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
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This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
Abb Vie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
About Abb Vie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
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AbbVie 소개

AbbVie
PublicPharmaceutical company.
10,001+
직원 수
North Chicago
본사 위치
$200B
기업 가치
리뷰
3.2
10개 리뷰
워라밸
3.2
보상
4.1
문화
2.8
커리어
2.9
경영진
2.3
45%
친구에게 추천
장점
Good compensation and benefits
Strong leadership potential
Good facilities and resources
단점
Poor management and leadership issues
Toxic work environment
Frequent policy and organizational changes
연봉 정보
88개 데이터
Junior/L3
Mid/L4
Director
Junior/L3 · Associate Manager, Promotion Analytics
1개 리포트
$144,943
총 연봉
기본급
$125,951
주식
-
보너스
-
$144,943
$144,943
면접 경험
4개 면접
난이도
3.0
/ 5
소요 기간
14-28주
경험
긍정 0%
보통 25%
부정 75%
면접 과정
1
Application Review
2
HR Screen
3
Hiring Manager Interview
4
Panel Interview
5
Offer
자주 나오는 질문
Behavioral/STAR
Past Experience
Culture Fit
Technical Knowledge
뉴스 & 버즈
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FDA Issues CRL to AbbVie | PharmExec - Pharmaceutical Executive
Pharmaceutical Executive
News
·
Today
FDA Issues Complete Response Letter for AbbVie’s Rapid-Onset Neurotoxin, TrenibotulinumtoxinE - Dermatology Times
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News
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Today